Canonical Allele Identifier: PA2825055340
Gene: FANCC HGNC NCBI

Linked Data

ClinVar Variation Id: 844720

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000127.2:p.Gly116Asp
CA374338916
NM_000136.3:c.347G>A