Allele Registry

Canonical Allele Identifier: PA125535

Gene: HBB HGNC NCBI

ClinVar RCV:

RCV000016882

ClinVar Variation:

15615

HGVS (amino-acid)	Matching Registered Transcripts
NP_000509.1:p.Gly30Ser	CA125534 NM_000518.5:c.88G>A