Allele Registry

Canonical Allele Identifier: PA355503

Gene: FANCC HGNC NCBI

ClinVar RCV:

RCV000204753

RCV000482871

RCV001025655

ClinVar Variation:

220497

HGVS (amino-acid)	Matching Registered Transcripts
NP_000127.2:p.Ile227Val	CA348958 NM_000136.3:c.679A>G