Allele Registry

Canonical Allele Identifier: PA257498

Gene: CFH HGNC NCBI

ClinVar RCV:

RCV000018010

ClinVar Variation:

16544

HGVS (amino-acid)	Matching Registered Transcripts
NP_000177.2:p.Cys959Tyr	CA257496 NM_000186.4:c.2876G>A