Allele Registry

Canonical Allele Identifier: PA2825083511

Gene: CFI HGNC NCBI

ClinVar RCV:

RCV002933147

RCV003326020

ClinVar Variation:

2055075

HGVS (amino-acid)	Matching Registered Transcripts
NP_000195.3:p.Pro64Leu	CA3042338 NM_000204.5:c.191C>T