Allele Registry

Canonical Allele Identifier: PA2828569155

Gene: CFI HGNC NCBI

ClinVar RCV:

RCV003555155

ClinVar Variation:

2734666

HGVS (amino-acid)	Matching Registered Transcripts
NP_001362212.1:p.Arg429Cys	CA3041934 NM_001375283.1:c.1285C>T