Canonical Allele Identifier: PA1139694182
Gene: FANCC HGNC NCBI

Linked Data

ClinVar Variation Id: 949422

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001230672.1:p.Glu521Ala
CA5137296
NM_001243743.2:c.1562A>C