Allele Registry

Canonical Allele Identifier: PA2828569072

Gene: CFI HGNC NCBI

ClinVar RCV:

RCV000012908

RCV001857336

RCV002496331

ClinVar Variation:

12125

HGVS (amino-acid)	Matching Registered Transcripts
NP_001362212.1:p.Arg298Trp	CA256220 NM_001375283.1:c.892C>T