Allele Registry

Canonical Allele Identifier: PA130023

Gene: HBB HGNC NCBI

ClinVar RCV:

RCV000030668

ClinVar Variation:

15327

HGVS (amino-acid)	Matching Registered Transcripts
NP_000509.1:p.Lys9Thr	CA130022 NM_000518.5:c.26A>C