Allele Registry

Canonical Allele Identifier: PA2828567697

Gene: CFI HGNC NCBI

ClinVar RCV:

RCV000012907

ClinVar Variation:

12124

HGVS (amino-acid)	Matching Registered Transcripts
NP_001362207.1:p.Gly243Asp	CA121905 NM_001375278.1:c.728G>A