Allele Registry

Canonical Allele Identifier: PA645402671

Gene: FANCC HGNC NCBI

ClinVar Allele:

407736

ClinVar RCV:

RCV000478222

RCV000702767

RCV001355099

RCV002413315

ClinVar Variation:

418189

HGVS (amino-acid)	Matching Registered Transcripts
NP_000127.2:p.Leu422Met	CA5137407 NM_000136.3:c.1264C>A