Allele Registry

Canonical Allele Identifier: PA125045

Gene: HBB HGNC NCBI

ClinVar RCV:

RCV000016502

ClinVar Variation:

15276

HGVS (amino-acid)	Matching Registered Transcripts
NP_000509.1:p.His93Arg	CA125044 NM_000518.5:c.278A>G