Allele Registry

Canonical Allele Identifier: PA916028676

Gene: CFI HGNC NCBI

ClinVar RCV:

RCV000055784

RCV000892174

RCV001171354

RCV002294012

RCV002496740

RCV004537251

ClinVar Variation:

65580

HGVS (amino-acid)	Matching Registered Transcripts
NP_001317964.1:p.Gly261Asp	CA344907 NM_001331035.2:c.782G>A