Allele Registry

Canonical Allele Identifier: PA126662

Gene: CFH HGNC NCBI

ClinVar RCV:

RCV000018017

RCV000190297

RCV000274380

RCV000331871

RCV000374816

RCV001579191

RCV002293982

ClinVar Variation:

16550

HGVS (amino-acid)	Matching Registered Transcripts
NP_000177.2:p.Val62Ile	CA126660 NM_000186.4:c.184G>A