Allele Registry

Canonical Allele Identifier: PA125089

Gene: HBB HGNC NCBI

ClinVar RCV:

RCV000016537

RCV000029964

RCV001811161

ClinVar Variation:

15302

HGVS (amino-acid)	Matching Registered Transcripts
NP_000509.1:p.Asp53Asn	CA125088 NM_000518.5:c.157G>A