Allele Registry

Canonical Allele Identifier: PA3057313254

Gene: CFH HGNC NCBI

ClinVar RCV:

RCV004788334

ClinVar Variation:

3376720

HGVS (amino-acid)	Matching Registered Transcripts
NP_000177.2:p.Arg1215Gln	CA343988235 NM_000186.4:c.3644G>A