Allele Registry

Canonical Allele Identifier: PA2573073588

Gene: CFI HGNC NCBI

ClinVar RCV:

RCV000012907

ClinVar Variation:

12124

HGVS (amino-acid)	Matching Registered Transcripts
NP_001362213.1:p.Gly40Asp	CA121905 NM_001375284.1:c.119G>A