Canonical Allele Identifier: PA104731
Gene: SH2D1A HGNC NCBI

Linked Data

ClinVar Variation Id: 10901
ClinVar RCV Id: RCV000011648
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002342.1:p.Arg32Thr
CA255595
NM_002351.5:c.95G>C