Allele Registry

Canonical Allele Identifier: PA2826329942

Gene: FANCC HGNC NCBI

ClinVar RCV:

RCV000115341

RCV000206060

RCV002381419

ClinVar Variation:

127531

HGVS (amino-acid)	Matching Registered Transcripts
NP_001230672.1:p.Arg433Cys	CA287184 NM_001243743.2:c.1297C>T