Allele Registry

Canonical Allele Identifier: PA2829587896

Gene: SH2B3 HGNC NCBI

ClinVar RCV:

RCV001667974

RCV002488461

ClinVar Variation:

1265448

HGVS (amino-acid)	Matching Registered Transcripts
NP_005466.1:p.Trp262Arg	CA6789733 NM_005475.3:c.784T>C CA386710508 NM_005475.3:c.784T>A