Allele Registry

Canonical Allele Identifier: PA129207

Gene: SH2B3 HGNC NCBI

ClinVar RCV:

RCV000023398

RCV000988910

RCV001529953

RCV001843460

RCV002466413

ClinVar Variation:

30445

HGVS (amino-acid)	Matching Registered Transcripts
NP_005466.1:p.Glu208Gln	CA129205 NM_005475.3:c.622G>C