Allele Registry

Canonical Allele Identifier: PA2826932765

Gene: SH2B1 HGNC NCBI

ClinVar RCV:

RCV001621215

ClinVar Variation:

1232867

HGVS (amino-acid)	Matching Registered Transcripts
NP_001295222.1:p.Thr484Ala	CA7986210 NM_001308293.2:c.1450A>G