Allele Registry

Canonical Allele Identifier: PA2827353001

Gene: CFI HGNC NCBI

ClinVar RCV:

RCV003555155

ClinVar Variation:

2734666

HGVS (amino-acid)	Matching Registered Transcripts
NP_001317964.1:p.Arg441Cys	CA3041934 NM_001331035.2:c.1321C>T