Allele Registry

Canonical Allele Identifier: PA125501

Gene: HBB HGNC NCBI

ClinVar RCV:

RCV000016857

ClinVar Variation:

15590

HGVS (amino-acid)	Matching Registered Transcripts
NP_000509.1:p.Gly137Arg	CA125500 NM_000518.5:c.409G>C