Allele Registry

Canonical Allele Identifier: PA2741816211

Gene: HBB HGNC NCBI

ClinVar RCV:

RCV003479690

ClinVar Variation:

2682317

HGVS (amino-acid)	Matching Registered Transcripts
NP_000509.1:p.Ala136Val	CA5839691 NM_000518.5:c.407C>T