Allele Registry

Canonical Allele Identifier: PA2825579465

Gene: SH2D1A HGNC NCBI

ClinVar RCV:

RCV001975588

ClinVar Variation:

1471227

HGVS (amino-acid)	Matching Registered Transcripts
NP_001108409.1:p.Pro125_Ter126insGlyArgLysIleLysHisLeuValLeuTyrPheLeu	CA414125200 NM_001114937.3:c.376T>G