Canonical Allele Identifier: PA2741893226
Gene: SH2D1A HGNC NCBI

Linked Data

ClinVar Variation Id: 2501803
ClinVar RCV Id: RCV003228222
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002342.1:p.His8Pro
CA414122208
NM_002351.5:c.23A>C