Allele Registry

Canonical Allele Identifier: PA124800

Gene: HBB HGNC NCBI

ClinVar RCV:

RCV000016302

ClinVar Variation:

15139

HGVS (amino-acid)	Matching Registered Transcripts
NP_000509.1:p.His147Arg	CA124799 NM_000518.5:c.440A>G