Allele Registry

Canonical Allele Identifier: PA2826932836

Gene: SH2B1 HGNC NCBI

ClinVar RCV:

RCV001621215

ClinVar Variation:

1232867

HGVS (amino-acid)	Matching Registered Transcripts
NP_001295223.1:p.Thr148Ala	CA7986210 NM_001308294.2:c.442A>G