Allele Registry

Canonical Allele Identifier: PA124777

Gene: HBB HGNC NCBI

ClinVar RCV:

RCV000016282

ClinVar Variation:

15124

HGVS (amino-acid)	Matching Registered Transcripts
NP_000509.1:p.Gly108Arg	CA124776 NM_000518.5:c.322G>C