Allele Registry

Canonical Allele Identifier: PA913194671

Gene: HBB HGNC NCBI

ClinVar RCV:

RCV000757366

ClinVar Variation:

618676

HGVS (amino-acid)	Matching Registered Transcripts
NP_000509.1:p.Asp53Val	CA217114308 NM_000518.5:c.158A>T