Allele Registry

Canonical Allele Identifier: PA2825084065

Gene: CFI HGNC NCBI

ClinVar Allele:

27165

ClinVar RCV:

RCV000012909

RCV002512998

ClinVar Variation:

12126

HGVS (amino-acid)	Matching Registered Transcripts
NP_000195.3:p.Asp519Asn	CA256223 NM_000204.5:c.1555G>A