Allele Registry

Canonical Allele Identifier: PA124938

Gene: HBB HGNC NCBI

ClinVar RCV:

RCV000016405

RCV001811154

ClinVar Variation:

15214

HGVS (amino-acid)	Matching Registered Transcripts
NP_000509.1:p.Gly57Asp	CA124937 NM_000518.5:c.170G>A