Allele Registry

Canonical Allele Identifier: PA125142

Gene: HBB HGNC NCBI

ClinVar RCV:

RCV000016582

RCV000641604

ClinVar Variation:

15339

HGVS (amino-acid)	Matching Registered Transcripts
NP_000509.1:p.Ala141Thr	CA125141 NM_000518.5:c.421G>A