Canonical Allele Identifier: PA2499242464
Gene: FANCC HGNC NCBI

Linked Data

ClinVar Variation Id: 1017642
ClinVar RCV Id: RCV001316820 RCV002384400 RCV002486246
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001230672.1:p.His452Arg
CA374106246
NM_001243743.2:c.1355A>G