Canonical Allele Identifier: PA1139694262
Gene: FANCC HGNC NCBI

Linked Data

ClinVar Variation Id: 949953

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001230672.1:p.Ala547Val
CA374104321
NM_001243743.2:c.1640C>T