Allele Registry

Canonical Allele Identifier: PA125450

Gene: HBB HGNC NCBI

ClinVar RCV:

RCV000016827

ClinVar Variation:

15561

HGVS (amino-acid)	Matching Registered Transcripts
NP_000509.1:p.Lys83Glu	CA125449 NM_000518.5:c.247A>G