Allele Registry

Canonical Allele Identifier: PA125121

Gene: HBB HGNC NCBI

ClinVar RCV:

RCV000016562

RCV000641598

RCV001284491

ClinVar Variation:

15322

HGVS (amino-acid)	Matching Registered Transcripts
NP_000509.1:p.Tyr146Cys	CA125120 NM_000518.5:c.437A>G