Allele Registry

Canonical Allele Identifier: PA125234

Gene: HBB HGNC NCBI

ClinVar RCV:

RCV000016641

ClinVar Variation:

15388

HGVS (amino-acid)	Matching Registered Transcripts
NP_000509.1:p.Tyr131Asp	CA125233 NM_000518.5:c.391T>G