Allele Registry

Canonical Allele Identifier: PA2828569134

Gene: CFI HGNC NCBI

ClinVar Allele:

27157

ClinVar RCV:

RCV000012901

RCV002465487

ClinVar Variation:

12118

HGVS (amino-acid)	Matching Registered Transcripts
NP_001362212.1:p.His399Leu	CA121902 NM_001375283.1:c.1196A>T