Allele Registry

Canonical Allele Identifier: PA124860

Gene: HBB HGNC NCBI

ClinVar RCV:

RCV000016351

ClinVar Variation:

15174

HGVS (amino-acid)	Matching Registered Transcripts
NP_000509.1:p.Asp80Gly	CA124859 NM_000518.5:c.239A>G