Canonical Allele Identifier: PA1139694424
Gene: FANCC HGNC NCBI

Linked Data

ClinVar Variation Id: 844720

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001230673.1:p.Gly116Asp
CA374338916
NM_001243744.2:c.347G>A