Canonical Allele Identifier: PA916006655
Gene: FANCC HGNC NCBI

Linked Data

ClinVar Variation Id: 182492

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001230672.1:p.Arg548Gln
CA299203
NM_001243743.2:c.1643G>A