Allele Registry

Canonical Allele Identifier: PA2826977632

Gene: CFI HGNC NCBI

ClinVar RCV:

RCV002933147

RCV003326020

ClinVar Variation:

2055075

HGVS (amino-acid)	Matching Registered Transcripts
NP_001304986.2:p.Pro64Leu	CA3042338 NM_001318057.2:c.191C>T