Allele Registry

Canonical Allele Identifier: PA916022203

Gene: CFI HGNC NCBI

ClinVar Allele:

27165

ClinVar RCV:

RCV000012909

RCV002512998

ClinVar Variation:

12126

HGVS (amino-acid)	Matching Registered Transcripts
NP_001304986.2:p.Asp527Asn	CA256223 NM_001318057.2:c.1579G>A