Allele Registry

Canonical Allele Identifier: PA124858

Gene: HBB HGNC NCBI

ClinVar RCV:

RCV000016348

RCV000016349

RCV000016350

RCV000507079

RCV002476973

ClinVar Variation:

15173

HGVS (amino-acid)	Matching Registered Transcripts
NP_000509.1:p.Glu44Ala	CA124857 NM_000518.5:c.131A>C