Allele Registry

Canonical Allele Identifier: PA645402332

Gene: FANCC HGNC NCBI

ClinVar RCV:

RCV000480272

RCV001276465

RCV002455910

ClinVar Variation:

418186

HGVS (amino-acid)	Matching Registered Transcripts
NP_000127.2:p.Ile80Val	CA16618894 NM_000136.3:c.238A>G