Canonical Allele Identifier: PA2825056244
Gene: FANCC HGNC NCBI

Linked Data

ClinVar Variation Id: 2450924
ClinVar RCV Id: RCV003177301

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000127.2:p.Arg542Gly
CA374104401
NM_000136.3:c.1624A>G