Allele Registry

Canonical Allele Identifier: PA125063

Gene: HBB HGNC NCBI

ClinVar RCV:

RCV000016519

ClinVar Variation:

15288

HGVS (amino-acid)	Matching Registered Transcripts
NP_000509.1:p.Glu44_Phe46del	CA125062 NM_000518.5:c.131_139del