Allele Registry

Canonical Allele Identifier: PA257505

Gene: CFH HGNC NCBI

ClinVar RCV:

RCV000018014

ClinVar Variation:

16548

HGVS (amino-acid)	Matching Registered Transcripts
NP_000177.2:p.Leu1189Arg	CA257503 NM_000186.4:c.3566T>G