Canonical Allele Identifier: PA658811751
Gene: SH3TC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 543360
ClinVar RCV Id: RCV000654108 RCV002424544
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_078853.2:p.Arg851Gln
CA3498970
NM_024577.4:c.2552G>A