Allele Registry

Canonical Allele Identifier: PA2741813003

Gene: CFH HGNC NCBI

ClinVar RCV:

RCV003361269

ClinVar Variation:

2595833

HGVS (amino-acid)	Matching Registered Transcripts
NP_000177.2:p.Asp855Asn	CA1305684 NM_000186.4:c.2563G>A