Canonical Allele Identifier: PA2580176454
Gene: FANCC HGNC NCBI

Linked Data

ClinVar Variation Id: 1770631
ClinVar RCV Id: RCV002387979

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001230672.1:p.Gly451Asp
CA374106252
NM_001243743.2:c.1352G>A