Allele Registry

Canonical Allele Identifier: PA125023

Gene: HBB HGNC NCBI

ClinVar RCV:

RCV000016487

ClinVar Variation:

15263

HGVS (amino-acid)	Matching Registered Transcripts
NP_000509.1:p.Met56Lys	CA125022 NM_000518.5:c.167T>A