Allele Registry

Canonical Allele Identifier: PA256209

Gene: FANCC HGNC NCBI

ClinVar Allele:

27089

ClinVar RCV:

RCV000012830

ClinVar Variation:

12050

HGVS (amino-acid)	Matching Registered Transcripts
NP_000127.2:p.Leu496Arg	CA256207 NM_000136.3:c.1487T>G