Allele Registry

Canonical Allele Identifier: PA124821

Gene: HBB HGNC NCBI

ClinVar RCV:

RCV000016313

RCV000506646

RCV001826463

ClinVar Variation:

15150

HGVS (amino-acid)	Matching Registered Transcripts
NP_000509.1:p.Thr88Lys	CA124820 NM_000518.5:c.263C>A