Allele Registry

Canonical Allele Identifier: PA2827353059

Gene: CFI HGNC NCBI

ClinVar Allele:

27165

ClinVar RCV:

RCV000012909

RCV002512998

ClinVar Variation:

12126

HGVS (amino-acid)	Matching Registered Transcripts
NP_001317964.1:p.Asp512Asn	CA256223 NM_001331035.2:c.1534G>A