Allele Registry

Canonical Allele Identifier: PA645425234

Gene: CFH HGNC NCBI

ClinVar RCV:

RCV000256395

ClinVar Variation:

265982

HGVS (amino-acid)	Matching Registered Transcripts
NP_000177.2:p.Cys984Arg	CA10588915 NM_000186.4:c.2950T>C