Allele Registry

Canonical Allele Identifier: PA125439

Gene: HBB HGNC NCBI

ClinVar RCV:

RCV000016820

ClinVar Variation:

15554

HGVS (amino-acid)	Matching Registered Transcripts
NP_000509.1:p.Glu27Gly	CA125438 NM_000518.5:c.80A>G