Canonical Allele Identifier: PA2826330623
Gene: FANCC HGNC NCBI

Linked Data

ClinVar Variation Id: 1304604

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001230672.1:p.Leu166Arg
CA5137720
NM_001243743.2:c.497T>G