Allele Registry

Canonical Allele Identifier: PA2829346372

Gene: SH2D1A HGNC NCBI

ClinVar RCV:

RCV001975588

ClinVar Variation:

1471227

HGVS (amino-acid)	Matching Registered Transcripts
NP_002342.1:p.Pro128_Ter129insGlyArgLysIleLysHisLeuValLeuTyrPheLeu	CA414125200 NM_002351.5:c.385T>G