Canonical Allele Identifier: PA2825056234
Gene: FANCC HGNC NCBI

Linked Data

ClinVar Variation Id: 1776444
ClinVar RCV Id: RCV002400940

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000127.2:p.Ile538Thr
CA374104466
NM_000136.3:c.1613T>C