Allele Registry

Canonical Allele Identifier: PA287186

Gene: FANCC HGNC NCBI

ClinVar RCV:

RCV000115341

RCV000206060

RCV002381419

ClinVar Variation:

127531

HGVS (amino-acid)	Matching Registered Transcripts
NP_000127.2:p.Arg433Cys	CA287184 NM_000136.3:c.1297C>T