Allele Registry

Canonical Allele Identifier: PA916006832

Gene: FANCC HGNC NCBI

ClinVar Allele:

132998

ClinVar RCV:

RCV000115352

RCV000315029

RCV000571052

RCV000709093

RCV001818267

RCV003492473

ClinVar Variation:

127541

HGVS (amino-acid)	Matching Registered Transcripts
NP_001230673.1:p.Ala132Gly	CA287213 NM_001243744.2:c.395C>G