Allele Registry

Canonical Allele Identifier: PA2499229564

Gene: CFH HGNC NCBI

ClinVar RCV:

RCV001328123

ClinVar Variation:

988141

HGVS (amino-acid)	Matching Registered Transcripts
NP_000177.2:p.Arg1182Ser	CA343987394 NM_000186.4:c.3546G>C CA343987399 NM_000186.4:c.3546G>T