Allele Registry

Canonical Allele Identifier: PA299147

Gene: FANCC HGNC NCBI

ClinVar Allele:

180352

ClinVar RCV:

RCV000160473

RCV000470152

RCV000564307

RCV000988216

RCV002271426

RCV002492634

ClinVar Variation:

182472

HGVS (amino-acid)	Matching Registered Transcripts
NP_000127.2:p.Arg185Gln	CA299145 NM_000136.3:c.554G>A