Allele Registry

Canonical Allele Identifier: PA336596

Gene: FANCC HGNC NCBI

ClinVar Allele:

212684

ClinVar RCV:

RCV000196637

RCV000709089

RCV001025536

RCV001818486

RCV002478703

ClinVar Variation:

216290

HGVS (amino-acid)	Matching Registered Transcripts
NP_000127.2:p.Val223Ala	CA336594 NM_000136.3:c.668T>C