Allele Registry

Canonical Allele Identifier: PA125214

Gene: HBB HGNC NCBI

ClinVar RCV:

RCV000016629

ClinVar Variation:

15377

HGVS (amino-acid)	Matching Registered Transcripts
NP_000509.1:p.Pro52Arg	CA125213 NM_000518.5:c.155C>G