Allele Registry

Canonical Allele Identifier: PA2741813056

Gene: CFH HGNC NCBI

ClinVar RCV:

RCV003481559

ClinVar Variation:

2682692

HGVS (amino-acid)	Matching Registered Transcripts
NP_000177.2:p.Asp1220Gly	CA1306000 NM_000186.4:c.3659A>G