Allele Registry

Canonical Allele Identifier: PA2825083881

Gene: CFI HGNC NCBI

ClinVar Allele:

27157

ClinVar RCV:

RCV000012901

RCV002465487

ClinVar Variation:

12118

HGVS (amino-acid)	Matching Registered Transcripts
NP_000195.3:p.His418Leu	CA121902 NM_000204.5:c.1253A>T