Canonical Allele Identifier: PA2573284433
Gene: SH3TC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1347096
ClinVar RCV Id: RCV002032978
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_078853.2:p.Ile981dup
CA2573139254
NM_024577.4:c.2942_2944dup