Allele Registry

Canonical Allele Identifier: PA125520

Gene: HBB HGNC NCBI

ClinVar RCV:

RCV000016872

ClinVar Variation:

15605

HGVS (amino-acid)	Matching Registered Transcripts
NP_000509.1:p.Val35Asp	CA125519 NM_000518.5:c.104T>A