Allele Registry

Canonical Allele Identifier: PA2825206145

Gene: HBB HGNC NCBI

ClinVar RCV:

RCV004547426

ClinVar Variation:

3235090

HGVS (amino-acid)	Matching Registered Transcripts
NP_000509.1:p.Ala129Thr	CA5839695 NM_000518.5:c.385G>A