Allele Registry

Canonical Allele Identifier: PA124942

Gene: HBB HGNC NCBI

ClinVar RCV:

RCV000016410

RCV000016411

RCV000016412

ClinVar Variation:

15216

HGVS (amino-acid)	Matching Registered Transcripts
NP_000509.1:p.Gly65Asp	CA124941 NM_000518.5:c.194G>A