Allele Registry

Canonical Allele Identifier: PA2826977667

Gene: CFI HGNC NCBI

ClinVar RCV:

RCV001150342

ClinVar Variation:

903200

HGVS (amino-acid)	Matching Registered Transcripts
NP_001304986.2:p.Gly125Arg	CA103697334 NM_001318057.2:c.373G>A CA357864062 NM_001318057.2:c.373G>C