Allele Registry

Canonical Allele Identifier: PA2826977846

Gene: CFI HGNC NCBI

ClinVar RCV:

RCV003555155

ClinVar Variation:

2734666

HGVS (amino-acid)	Matching Registered Transcripts
NP_001304986.2:p.Arg456Cys	CA3041934 NM_001318057.2:c.1366C>T