Allele Registry

Canonical Allele Identifier: PA2499235181

Gene: CFH HGNC NCBI

ClinVar Allele:

1151870

ClinVar RCV:

RCV001507513

ClinVar Variation:

1162888

HGVS (amino-acid)	Matching Registered Transcripts
NP_001014975.1:p.Arg257Cys	CA1305140 NM_001014975.3:c.769C>T