Allele Registry

Canonical Allele Identifier: PA125000

Gene: HBB HGNC NCBI

ClinVar RCV:

RCV000016455

RCV000016456

ClinVar Variation:

15249

HGVS (amino-acid)	Matching Registered Transcripts
NP_000509.1:p.Pro37Thr	CA124999 NM_000518.5:c.109C>A