Canonical Allele Identifier: PA299205
Gene: FANCC HGNC NCBI

Linked Data

ClinVar Variation Id: 182492

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000127.2:p.Arg548Gln
CA299203
NM_000136.3:c.1643G>A