Allele Registry

Canonical Allele Identifier: PA104888

Gene: SH2D1A HGNC NCBI

ClinVar RCV:

RCV000011652

ClinVar Variation:

10905

HGVS (amino-acid)	Matching Registered Transcripts
NP_002342.1:p.Thr68Ile	CA255602 NM_002351.5:c.203C>T