Allele Registry

Canonical Allele Identifier: PA125429

Gene: HBB HGNC NCBI

ClinVar RCV:

RCV000016814

ClinVar Variation:

15548

HGVS (amino-acid)	Matching Registered Transcripts
NP_000509.1:p.Lys9Met	CA125428 NM_000518.5:c.26A>T