Allele Registry

Canonical Allele Identifier: PA124833

Gene: HBB HGNC NCBI

ClinVar RCV:

RCV000016326

ClinVar Variation:

15158

HGVS (amino-acid)	Matching Registered Transcripts
NP_000509.1:p.Val99Ala	CA124832 NM_000518.5:c.296T>C