Allele Registry

Canonical Allele Identifier: PA124966

Gene: HBB HGNC NCBI

ClinVar RCV:

RCV000016426

RCV000016429

ClinVar Variation:

15228

HGVS (amino-acid)	Matching Registered Transcripts
NP_000509.1:p.Ala130Asp	CA124965 NM_000518.5:c.389C>A