Allele Registry

Canonical Allele Identifier: PA2827352917

Gene: CFI HGNC NCBI

ClinVar RCV:

RCV000012908

RCV001857336

RCV002496331

ClinVar Variation:

12125

HGVS (amino-acid)	Matching Registered Transcripts
NP_001317964.1:p.Arg310Trp	CA256220 NM_001331035.2:c.928C>T