Canonical Allele Identifier: PA2580264420
Gene: SH2D1A HGNC NCBI

Linked Data

ClinVar Variation Id: 2442798
ClinVar RCV Id: RCV003150604
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002342.1:p.Met1Val