Canonical Allele Identifier: PA2580176521
Gene: FANCC HGNC NCBI

Linked Data

ClinVar Variation Id: 1777282
ClinVar RCV Id: RCV002403680

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001230672.1:p.Leu551His
CA374104266
NM_001243743.2:c.1652T>A