Allele Registry

Canonical Allele Identifier: PA2741872682

Gene: CFI HGNC NCBI

ClinVar RCV:

RCV003555155

ClinVar Variation:

2734666

HGVS (amino-acid)	Matching Registered Transcripts
NP_001362207.1:p.Arg456Cys	CA3041934 NM_001375278.1:c.1366C>T