Allele Registry

Canonical Allele Identifier: PA125363

Gene: HBB HGNC NCBI

ClinVar RCV:

RCV000016763

ClinVar Variation:

15501

HGVS (amino-acid)	Matching Registered Transcripts
NP_000509.1:p.Glu122Gly	CA125362 NM_000518.5:c.365A>G