Allele Registry

Canonical Allele Identifier: PA125008

Gene: HBB HGNC NCBI

ClinVar RCV:

RCV000016462

RCV000641512

ClinVar Variation:

15254

HGVS (amino-acid)	Matching Registered Transcripts
NP_000509.1:p.Val68Glu	CA125007 NM_000518.5:c.203T>A