NM_002641.3:c.1077_1078delinsC

HGVS Expressions

  • NG_009786.1:g.15763_15764delinsC
  • NM_002641.3:c.1077_1078delinsC
  • NP_002632.1:p.Leu359PhefsTer8
  • NC_000023.11:g.15324775_15324776delinsG
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Variant Type

Indel

Epidemiology in the Arab World

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Subject IDCountry of OriginAllele CountAllele FrequencyCTGA Clinical Significance Condition(s)ReferenceRemarks
605988.GUnited Arab EmiratesAlmarzooqi et al. 2021 Study on symptomatic and asymptomatic Em...
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