Allele Registry

Canonical Allele Identifier: PA124905

Gene: HBB HGNC NCBI

ClinVar RCV:

RCV000016380

RCV000757357

RCV001277081

ClinVar Variation:

15197

HGVS (amino-acid)	Matching Registered Transcripts
NP_000509.1:p.Ala141Asp	CA124904 NM_000518.5:c.422C>A