Allele Registry

Canonical Allele Identifier: PA2825096384

Gene: CFH HGNC NCBI

ClinVar RCV:

RCV001898727

RCV002478327

RCV003452116

RCV003452117

RCV003452118

RCV003452119

ClinVar Variation:

1403152

HGVS (amino-acid)	Matching Registered Transcripts
NP_000177.2:p.Ser159Asn	CA1305072 NM_000186.4:c.476G>A