Allele Registry

Canonical Allele Identifier: PA124897

Gene: HBB HGNC NCBI

ClinVar RCV:

RCV000016376

RCV000641463

RCV001811153

ClinVar Variation:

15193

HGVS (amino-acid)	Matching Registered Transcripts
NP_000509.1:p.Lys83Met	CA124896 NM_000518.5:c.248A>T