Allele Registry

Canonical Allele Identifier: PA125417

Gene: HBB HGNC NCBI

ClinVar RCV:

RCV000016803

RCV000016804

ClinVar Variation:

15538

HGVS (amino-acid)	Matching Registered Transcripts
NP_000509.1:p.Gly26del	CA125416 NM_000518.5:c.77_79del