Allele Registry

Canonical Allele Identifier: PA342878

Gene: HBB HGNC NCBI

ClinVar RCV:

RCV000030006

RCV000506003

ClinVar Variation:

36337

HGVS (amino-acid)	Matching Registered Transcripts
NP_000509.1:p.Arg31Lys	CA342877 NM_000518.5:c.92G>A