Allele Registry

Canonical Allele Identifier: PA3057521122

Gene: CFI HGNC NCBI

ClinVar Allele:

3803660

ClinVar RCV:

RCV005145377

ClinVar Variation:

3671522

HGVS (amino-acid)	Matching Registered Transcripts
NP_001362213.1:p.Glu87Asp	CA3042149 NM_001375284.1:c.261A>C CA357860991 NM_001375284.1:c.261A>T