Allele Registry

Canonical Allele Identifier: PA2825096278

Gene: CFH HGNC NCBI

ClinVar Allele:

1966010

ClinVar RCV:

RCV002600163

ClinVar Variation:

1909237

HGVS (amino-acid)	Matching Registered Transcripts
NP_000177.2:p.Leu4Pro	CA343988826 NM_000186.4:c.11T>C