Canonical Allele Identifier: PA104739
Gene: SH2D1A HGNC NCBI

Linked Data

ClinVar Variation Id: 10910
ClinVar RCV Id: RCV000011657
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002342.1:p.Arg55Leu
CA255607
NM_002351.5:c.164G>T