Allele Registry

Canonical Allele Identifier: PA125222

Gene: HBB HGNC NCBI

ClinVar RCV:

RCV000016634

ClinVar Variation:

15382

HGVS (amino-acid)	Matching Registered Transcripts
NP_000509.1:p.Asp74Tyr	CA125221 NM_000518.5:c.220G>T