Allele Registry

Canonical Allele Identifier: PA2741825187

Gene: CFH HGNC NCBI

ClinVar Allele:

2898394

ClinVar RCV:

RCV003562319

ClinVar Variation:

2734061

HGVS (amino-acid)	Matching Registered Transcripts
NP_001014975.1:p.Lys82Arg	CA1304999 NM_001014975.3:c.245A>G