Allele Registry

Canonical Allele Identifier: PA124835

Gene: HBB HGNC NCBI

ClinVar RCV:

RCV000016327

ClinVar Variation:

15159

HGVS (amino-acid)	Matching Registered Transcripts
NP_000509.1:p.Val2Glu	CA124834 NM_000518.5:c.5T>A