Allele Registry

Canonical Allele Identifier: PA124972

Gene: HBB HGNC NCBI

ClinVar RCV:

RCV000016430

RCV001811156

ClinVar Variation:

15232

HGVS (amino-acid)	Matching Registered Transcripts
NP_000509.1:p.Gly47Glu	CA124971 NM_000518.5:c.140G>A