Allele Registry

Canonical Allele Identifier: PA125135

Gene: HBB HGNC NCBI

ClinVar RCV:

RCV000016571

ClinVar Variation:

15331

HGVS (amino-acid)	Matching Registered Transcripts
NP_000509.1:p.Trp38Arg	CA125134 NM_000518.5:c.112T>A CA217114578 NM_000518.5:c.112T>C