Allele Registry

Canonical Allele Identifier: PA124884

Gene: HBB HGNC NCBI

ClinVar RCV:

RCV000016366

RCV000016367

ClinVar Variation:

15186

HGVS (amino-acid)	Matching Registered Transcripts
NP_000509.1:p.Gln128Glu	CA124883 NM_000518.5:c.382C>G