Allele Registry

Canonical Allele Identifier: PA125004

Gene: HBB HGNC NCBI

ClinVar RCV:

RCV000016460

ClinVar Variation:

15252

HGVS (amino-acid)	Matching Registered Transcripts
NP_000509.1:p.Gly30Asp	CA125003 NM_000518.5:c.89G>A