Canonical Allele Identifier: PA287198
Gene: FANCC HGNC NCBI

Linked Data

ClinVar Variation Id: 127535

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000127.2:p.Arg535His
CA287196
NM_000136.3:c.1604G>A