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There are one genomic locations for TYR c.346C>T p

Location (GRCh38) Variation dbSNP ClinVar
NC_000011.10: 89,178,298 NM_000372.5:c.346C>T NM_000372.5(TYR):c.346C>T (p.Arg116Ter)
  • No items found.