Allele Registry

Canonical Allele Identifier: PA2573164296

Gene: CFH HGNC NCBI

ClinVar Allele:

1668490

ClinVar RCV:

RCV002222771

RCV003454039

RCV003454040

RCV003454041

RCV003456281

ClinVar Variation:

1676855

HGVS (amino-acid)	Matching Registered Transcripts
NP_000177.2:p.Arg582His	CA1305477 NM_000186.4:c.1745G>A