Allele Registry

Canonical Allele Identifier: PA124829

Gene: HBB HGNC NCBI

ClinVar RCV:

RCV000016324

RCV001811150

ClinVar Variation:

15156

HGVS (amino-acid)	Matching Registered Transcripts
NP_000509.1:p.His3Arg	CA124828 NM_000518.5:c.8A>G