Allele Registry

Canonical Allele Identifier: PA916022189

Gene: CFI HGNC NCBI

ClinVar RCV:

RCV000012908

RCV001857336

RCV002496331

ClinVar Variation:

12125

HGVS (amino-acid)	Matching Registered Transcripts
NP_001304986.2:p.Arg325Trp	CA256220 NM_001318057.2:c.973C>T