Allele Registry

Canonical Allele Identifier: PA257495

Gene: CFH HGNC NCBI

ClinVar RCV:

RCV000018009

ClinVar Variation:

16543

HGVS (amino-acid)	Matching Registered Transcripts
NP_000177.2:p.Cys536Arg	CA257493 NM_000186.4:c.1606T>C