Allele Registry

Canonical Allele Identifier: PA124763

Gene: HBB HGNC NCBI

ClinVar RCV:

RCV000016272

RCV000016273

RCV000641416

ClinVar Variation:

15117

HGVS (amino-acid)	Matching Registered Transcripts
NP_000509.1:p.Leu69His	CA124762 NM_000518.5:c.206T>A