Allele Registry

Canonical Allele Identifier: PA125083

Gene: HBB HGNC NCBI

ClinVar RCV:

RCV000016531

RCV003476896

ClinVar Variation:

15298

HGVS (amino-acid)	Matching Registered Transcripts
NP_000509.1:p.Leu142Arg	CA125082 NM_000518.5:c.425T>G