Allele Registry

Canonical Allele Identifier: PA2828569238

Gene: CFI HGNC NCBI

ClinVar Variation Id: 438686

HGVS (amino-acid)	Matching Registered Transcripts
NP_001362212.1:p.Ser551Thr	CA3041835 NM_001375283.1:c.1652G>C