Allele Registry

Canonical Allele Identifier: PA2825096403

Gene: CFH HGNC NCBI

ClinVar RCV:

RCV001866874

RCV002503384

RCV003451989

RCV003451990

RCV003451991

RCV003451992

ClinVar Variation:

1355349

HGVS (amino-acid)	Matching Registered Transcripts
NP_000177.2:p.Glu189Lys	CA1305090 NM_000186.4:c.565G>A