Allele Registry

Canonical Allele Identifier: PA125165

Gene: HBB HGNC NCBI

ClinVar RCV:

RCV000016597

RCV000507183

ClinVar Variation:

15351

HGVS (amino-acid)	Matching Registered Transcripts
NP_000509.1:p.Arg105Thr	CA125164 NM_000518.5:c.314G>C