Allele Registry

Canonical Allele Identifier: PA125012

Gene: HBB HGNC NCBI

ClinVar RCV:

RCV000016466

RCV000641524

RCV000988480

RCV001266995

ClinVar Variation:

15256

HGVS (amino-acid)	Matching Registered Transcripts
NP_000509.1:p.His64Tyr	CA125011 NM_000518.5:c.190C>T