Allele Registry

Canonical Allele Identifier: PA916022196

Gene: CFI HGNC NCBI

ClinVar Allele:

27157

ClinVar RCV:

RCV000012901

RCV002465487

ClinVar Variation:

12118

HGVS (amino-acid)	Matching Registered Transcripts
NP_001304986.2:p.His426Leu	CA121902 NM_001318057.2:c.1277A>T