Allele Registry

Canonical Allele Identifier: PA125150

Gene: HBB HGNC NCBI

ClinVar RCV:

RCV000016586

RCV000757364

RCV003137530

ClinVar Variation:

15343

HGVS (amino-acid)	Matching Registered Transcripts
NP_000509.1:p.Leu89Pro	CA125149 NM_000518.5:c.266T>C