Allele Registry

Canonical Allele Identifier: PA2827353060

Gene: CFI HGNC NCBI

ClinVar Allele:

3395098

ClinVar RCV:

RCV004555240

ClinVar Variation:

3235979

HGVS (amino-acid)	Matching Registered Transcripts
NP_001317964.1:p.Asp517Gly	CA357854665 NM_001331035.2:c.1550A>G