Allele Registry

Canonical Allele Identifier: PA915958310

Gene: HBB HGNC NCBI

ClinVar RCV:

RCV001002299

ClinVar Variation:

811863

HGVS (amino-acid)	Matching Registered Transcripts
NP_000509.1:p.Asn103Asp	CA379273765 NM_000518.5:c.307A>G