Allele Registry

Canonical Allele Identifier: PA913194665

Gene: HBB HGNC NCBI

ClinVar RCV:

RCV000759791

ClinVar Variation:

619853

HGVS (amino-acid)	Matching Registered Transcripts
NP_000509.1:p.Glu44Gly	CA217114448 NM_000518.5:c.131A>G