Allele Registry

Canonical Allele Identifier: PA913194724

Gene: HBB HGNC NCBI

ClinVar RCV:

RCV000781441

RCV001839458

ClinVar Variation:

633256

HGVS (amino-acid)	Matching Registered Transcripts
NP_000509.1:p.Tyr146Asn	CA217112211 NM_000518.5:c.436T>A