NM_001277115.1:c.9238C>A

HGVS Expressions

  • NG_012886.2:g.235687C>A
  • NM_001277115.1:c.9238C>A
  • NP_001264044.1:p.Leu3080Met
  • NC_000007.14:g.21773901C>A
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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
147060.3United Arab Emirates1Alsamri et al. 2020 Atopy reported in family
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