Allele Registry

Canonical Allele Identifier: PA124819

Gene: HBB HGNC NCBI

ClinVar RCV:

RCV000016312

RCV000759803

RCV002490376

ClinVar Variation:

15149

HGVS (amino-acid)	Matching Registered Transcripts
NP_000509.1:p.Glu23Val	CA124818 NM_000518.5:c.68A>T