Allele Registry

Canonical Allele Identifier: PA2499229565

Gene: CFH HGNC NCBI

ClinVar RCV:

RCV001530205

ClinVar Variation:

1175202

HGVS (amino-acid)	Matching Registered Transcripts
NP_000177.2:p.Trp1183Leu	CA343987433 NM_000186.4:c.3548G>T