Allele Registry

Canonical Allele Identifier: PA2573073590

Gene: CFI HGNC NCBI

ClinVar Allele:

76488

ClinVar RCV:

RCV000055784

RCV000892174

RCV001171354

RCV002294012

RCV002496740

RCV004537251

ClinVar Variation:

65580

HGVS (amino-acid)	Matching Registered Transcripts
NP_001362213.1:p.Gly58Asp	CA344907 NM_001375284.1:c.173G>A