Allele Registry

Canonical Allele Identifier: PA2580126514

Gene: HBB HGNC NCBI

ClinVar RCV:

RCV000016633

ClinVar Variation:

15381

HGVS (amino-acid)	Matching Registered Transcripts
NP_000509.1:p.Gln40Glu	CA217114554 NM_000518.5:c.118C>G