Allele Registry

Canonical Allele Identifier: PA125069

Gene: HBB HGNC NCBI

ClinVar RCV:

RCV000016523

ClinVar Variation:

15291

HGVS (amino-acid)	Matching Registered Transcripts
NP_000509.1:p.Val99Gly	CA125068 NM_000518.5:c.296T>G