Allele Registry

Canonical Allele Identifier: PA125541

Gene: HBB HGNC NCBI

ClinVar RCV:

RCV000016887

ClinVar Variation:

15620

HGVS (amino-acid)	Matching Registered Transcripts
NP_000509.1:p.Asp95Tyr	CA125540 NM_000518.5:c.283G>T