Allele Registry

Canonical Allele Identifier: PA125491

Gene: HBB HGNC NCBI

ClinVar RCV:

RCV000016851

RCV001563767

RCV001778656

RCV002482877

ClinVar Variation:

15584

HGVS (amino-acid)	Matching Registered Transcripts
NP_000509.1:p.Thr124Asn	CA125490 NM_000518.5:c.371C>A