Allele Registry

Canonical Allele Identifier: PA916006585

Gene: FANCC HGNC NCBI

ClinVar RCV:

RCV000012830

ClinVar Variation:

12050

HGVS (amino-acid)	Matching Registered Transcripts
NP_001230672.1:p.Leu496Arg	CA256207 NM_001243743.2:c.1487T>G