Allele Registry

Canonical Allele Identifier: PA2828568634

Gene: CFI HGNC NCBI

ClinVar RCV:

RCV003555155

ClinVar Variation:

2734666

HGVS (amino-acid)	Matching Registered Transcripts
NP_001362210.1:p.Arg448Cys	CA3041934 NM_001375281.1:c.1342C>T