Allele Registry

Canonical Allele Identifier: PA2580107652

Gene: CFH HGNC NCBI

ClinVar RCV:

RCV002294686

ClinVar Variation:

1712431

HGVS (amino-acid)	Matching Registered Transcripts
NP_000177.2:p.Arg1215Leu	CA343988240 NM_000186.4:c.3644G>T