Canonical Allele Identifier: PA916007147
Gene: FANCC HGNC NCBI

Linked Data

ClinVar Variation Id: 418852
ClinVar RCV Id: RCV000485470 RCV000570574 RCV000630858 RCV001274615 RCV002222522
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001230673.1:p.Ala415Val
CA16618879
NM_001243744.2:c.1244C>T