Allele Registry

Canonical Allele Identifier: PA2499281394

Gene: SH2B1 HGNC NCBI

ClinVar RCV:

RCV001621215

ClinVar Variation:

1232867

HGVS (amino-acid)	Matching Registered Transcripts
NP_056318.2:p.Thr484Ala	CA7986210 NM_015503.3:c.1450A>G