Mutation Details for c.926C>T
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cDNA Name
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c.926C>T
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Protein Name
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p.Ala309Val
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Exon or Intron
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exon 8
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Legacy Exon or Intron
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exon 7
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A309V
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Other Details
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Contributors
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Ferec C.
2002-01-01
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Institute
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Centre de Transfusion Sanguine et de Biogenetique Brest, France
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Submitted Phenotype Details
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The mutation was identified in an individual with persistent neonatal hypertrypsinemia. (pers. corr. Ferec)
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Reference
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To check if there are any papers published about this mutation/variant on PubMed, please click here.
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