Allele Registry

Canonical Allele Identifier: PA126672

Gene: CFH HGNC NCBI

ClinVar RCV:

RCV000018029

RCV001723576

ClinVar Variation:

16561

HGVS (amino-acid)	Matching Registered Transcripts
NP_000177.2:p.Arg1078Ser	CA126670 NM_000186.4:c.3234G>T CA343983674 NM_000186.4:c.3234G>C