Allele Registry

Canonical Allele Identifier: PA125483

Gene: HBB HGNC NCBI

ClinVar RCV:

RCV000016846

RCV000759063

ClinVar Variation:

15579

HGVS (amino-acid)	Matching Registered Transcripts
NP_000509.1:p.Thr85Ala	CA125482 NM_000518.5:c.253A>G