Canonical Allele Identifier: PA916006630
Gene: FANCC HGNC NCBI

Linked Data

ClinVar Variation Id: 220016
ClinVar RCV Id: RCV000205662 RCV000564875 RCV001753610 RCV003407725
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001230672.1:p.Arg535Cys
CA349793
NM_001243743.2:c.1603C>T