Allele Registry

Canonical Allele Identifier: PA2828569349

Gene: CFI HGNC NCBI

ClinVar RCV:

RCV003555155

ClinVar Variation:

2734666

HGVS (amino-acid)	Matching Registered Transcripts
NP_001362213.1:p.Arg245Cys	CA3041934 NM_001375284.1:c.733C>T