Allele Registry

Canonical Allele Identifier: PA125365

Gene: HBB HGNC NCBI

ClinVar RCV:

RCV000016764

ClinVar Variation:

15502

HGVS (amino-acid)	Matching Registered Transcripts
NP_000509.1:p.Cys113Tyr	CA125364 NM_000518.5:c.338G>A