Canonical Allele Identifier: PA2825055448
Gene: FANCC HGNC NCBI

Linked Data

ClinVar Variation Id: 1304604

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000127.2:p.Leu166Arg
CA5137720
NM_000136.3:c.497T>G