Canonical Allele Identifier: PA2825056060
Gene: FANCC HGNC NCBI

Linked Data

ClinVar Variation Id: 1770631
ClinVar RCV Id: RCV002387979

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000127.2:p.Gly451Asp
CA374106252
NM_000136.3:c.1352G>A