Allele Registry

Canonical Allele Identifier: PA124846

Gene: HBB HGNC NCBI

ClinVar RCV:

RCV000016339

ClinVar Variation:

15167

HGVS (amino-acid)	Matching Registered Transcripts
NP_000509.1:p.His3Tyr	CA124845 NM_000518.5:c.7C>T