Allele Registry

Canonical Allele Identifier: PA125469

Gene: HBB HGNC NCBI

ClinVar RCV:

RCV000016839

ClinVar Variation:

15572

HGVS (amino-acid)	Matching Registered Transcripts
NP_000509.1:p.Lys9Arg	CA125468 NM_000518.5:c.26A>G