Allele Registry

Canonical Allele Identifier: PA915956515

Gene: CFH HGNC NCBI

ClinVar RCV:

RCV000297641

RCV000312490

RCV000336891

RCV000406363

RCV001859772

RCV002294223

ClinVar Variation:

294487

HGVS (amino-acid)	Matching Registered Transcripts
NP_001014975.1:p.Arg257His	CA1305141 NM_001014975.3:c.770G>A