Allele Registry

Canonical Allele Identifier: PA2825579447

Gene: SH2D1A HGNC NCBI

ClinVar RCV:

RCV000011652

ClinVar Variation:

10905

HGVS (amino-acid)	Matching Registered Transcripts
NP_001108409.1:p.Thr68Ile	CA255602 NM_001114937.3:c.203C>T