Allele Registry

Canonical Allele Identifier: PA2826330219

Gene: FANCC HGNC NCBI

ClinVar Allele:

180362

ClinVar RCV:

RCV000160497

RCV001831983

RCV002426792

RCV002484995

ClinVar Variation:

182495

HGVS (amino-acid)	Matching Registered Transcripts
NP_001230672.1:p.Ile80Thr	CA299212 NM_001243743.2:c.239T>C