Allele Registry

Canonical Allele Identifier: PA916006955

Gene: FANCC HGNC NCBI

ClinVar RCV:

RCV000196637

RCV000709089

RCV001025536

RCV001818486

RCV002478703

ClinVar Variation:

216290

HGVS (amino-acid)	Matching Registered Transcripts
NP_001230673.1:p.Val223Ala	CA336594 NM_001243744.2:c.668T>C