NM_018676.4:c.1091G>A

HGVS Expressions

  • NG_047168.1:g.25378G>A
  • NM_018676.4:c.1091G>A
  • NP_061146.1:p.Arg364His
  • NC_000013.11:g.52386117C>T
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Variant Type

Substitution

Epidemiology in the Arab World

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Subject IDCountry of OriginAllele CountAllele FrequencyCTGA Clinical Significance Condition(s)ReferenceRemarks
147557.G.1Saudi Arabia2Monies et al. 2017 Couple with heterozygous variants in ITG...
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