Allele Registry

Canonical Allele Identifier: PA124936

Gene: HBB HGNC NCBI

ClinVar RCV:

RCV000016400

RCV000755547

ClinVar Variation:

15213

HGVS (amino-acid)	Matching Registered Transcripts
NP_000509.1:p.Gly17Asp	CA124935 NM_000518.5:c.50G>A