Allele Registry

Canonical Allele Identifier: PA2825083926

Gene: CFI HGNC NCBI

ClinVar RCV:

RCV003555155

ClinVar Variation:

2734666

HGVS (amino-acid)	Matching Registered Transcripts
NP_000195.3:p.Arg448Cys	CA3041934 NM_000204.5:c.1342C>T