Allele Registry

Canonical Allele Identifier: PA916007133

Gene: FANCC HGNC NCBI

ClinVar RCV:

RCV000205129

RCV000484234

RCV001010059

ClinVar Variation:

220210

HGVS (amino-acid)	Matching Registered Transcripts
NP_001230673.1:p.Gly388Arg	CA349330 NM_001243744.2:c.1162G>A CA374107573 NM_001243744.2:c.1162G>C