Allele Registry

Canonical Allele Identifier: PA125353

Gene: HBB HGNC NCBI

ClinVar RCV:

RCV000016751

ClinVar Variation:

15491

HGVS (amino-acid)	Matching Registered Transcripts
NP_000509.1:p.Leu29Arg	CA125352 NM_000518.5:c.86T>G