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There are two genomic locations for TKFC c.598G>A p

Location (GRCh38) Variation dbSNP ClinVar
NC_000011.10: 61,341,854 NM_001351979.2:c.598G>A 149571662 not reported
NC_000011.10: 61,342,786 NM_001351980.2:c.598G>A 1477806362 not reported
  • No items found.