Allele Registry

Canonical Allele Identifier: PA342869

Gene: HBB HGNC NCBI

ClinVar RCV:

RCV000586298

RCV002222359

ClinVar Variation:

36324

HGVS (amino-acid)	Matching Registered Transcripts
NP_000509.1:p.His118Arg	CA342868 NM_000518.5:c.353A>G