Allele Registry

Canonical Allele Identifier: PA2825096342

Gene: CFH HGNC NCBI

ClinVar RCV:

RCV003562319

ClinVar Variation:

2734061

HGVS (amino-acid)	Matching Registered Transcripts
NP_000177.2:p.Lys82Arg	CA1304999 NM_000186.4:c.245A>G