Allele Registry

Canonical Allele Identifier: PA2825579457

Gene: SH2D1A HGNC NCBI

ClinVar RCV:

RCV000011651

ClinVar Variation:

10904

HGVS (amino-acid)	Matching Registered Transcripts
NP_001108409.1:p.Pro101Leu	CA255600 NM_001114937.3:c.302C>T