Allele Registry

Canonical Allele Identifier: PA645425121

Gene: CFH HGNC NCBI

ClinVar Allele:

279193

ClinVar RCV:

RCV000297641

RCV000312490

RCV000336891

RCV000406363

RCV001859772

RCV002294223

ClinVar Variation:

294487

HGVS (amino-acid)	Matching Registered Transcripts
NP_000177.2:p.Arg257His	CA1305141 NM_000186.4:c.770G>A