Allele Registry

Canonical Allele Identifier: PA125351

Gene: HBB HGNC NCBI

ClinVar RCV:

RCV000016750

ClinVar Variation:

15490

HGVS (amino-acid)	Matching Registered Transcripts
NP_000509.1:p.Val55Asp	CA125350 NM_000518.5:c.164T>A