Allele Registry

Canonical Allele Identifier: PA125129

Gene: HBB HGNC NCBI

ClinVar RCV:

RCV000016567

ClinVar Variation:

15328

HGVS (amino-acid)	Matching Registered Transcripts
NP_000509.1:p.Gly25Arg	CA125128 NM_000518.5:c.73G>C