Allele Registry

Canonical Allele Identifier: PA124784

Gene: HBB HGNC NCBI

ClinVar RCV:

RCV000016294

RCV001283991

ClinVar Variation:

15131

HGVS (amino-acid)	Matching Registered Transcripts
NP_000509.1:p.Leu92Arg	CA124783 NM_000518.5:c.275T>G