Allele Registry

Canonical Allele Identifier: PA2826977898

Gene: CFI HGNC NCBI

ClinVar Allele:

3395098

ClinVar RCV:

RCV004555240

ClinVar Variation:

3235979

HGVS (amino-acid)	Matching Registered Transcripts
NP_001304986.2:p.Asp532Gly	CA357854665 NM_001318057.2:c.1595A>G