Allele Registry

Canonical Allele Identifier: PA104855

Gene: SH2D1A HGNC NCBI

ClinVar RCV:

RCV000011651

ClinVar Variation:

10904

HGVS (amino-acid)	Matching Registered Transcripts
NP_002342.1:p.Pro101Leu	CA255600 NM_002351.5:c.302C>T