Allele Registry

Canonical Allele Identifier: PA2827353084

Gene: CFI HGNC NCBI

ClinVar Variation Id: 438686

HGVS (amino-acid)	Matching Registered Transcripts
NP_001317964.1:p.Ser563Thr	CA3041835 NM_001331035.2:c.1688G>C