Allele Registry

Canonical Allele Identifier: PA299186

Gene: FANCC HGNC NCBI

ClinVar Allele:

180337

ClinVar RCV:

RCV000160486

RCV000477242

RCV000570128

RCV001273988

RCV001358089

ClinVar Variation:

182485

HGVS (amino-acid)	Matching Registered Transcripts
NP_000127.2:p.Glu417Lys	CA299184 NM_000136.3:c.1249G>A