Allele Registry

Canonical Allele Identifier: PA099276

Gene: HBB HGNC NCBI

ClinVar RCV:

RCV000016791

RCV002284172

ClinVar Variation:

15526

HGVS (amino-acid)	Matching Registered Transcripts
NP_000509.1:p.Ala116Asp	CA125396 NM_000518.5:c.347C>A