Allele Registry

Canonical Allele Identifier: PA257508

Gene: CFH HGNC NCBI

ClinVar RCV:

RCV000018018

ClinVar Variation:

16551

HGVS (amino-acid)	Matching Registered Transcripts
NP_000177.2:p.Cys431Ser	CA257506 NM_000186.4:c.1291T>A CA343980786 NM_000186.4:c.1292G>C