NM_005518.4:c.754A>G

HGVS Expressions

  • NG_013348.1:g.14719A>G
  • NM_005518.4:c.754A>G
  • NP_005509.1:p.Ile252Val
  • NC_000001.11:g.119759214T>C
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CTGA Clinical Significance

Uncertain Significance

Variant Type

Substitution

Epidemiology in the Arab World

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Subject IDCountry of OriginAllele CountAllele FrequencyCTGA Clinical Significance Condition(s)ReferenceRemarks
178500.2.1United Arab Emirates1Uncertain SignificanceAlsamri et al. 2020; Alsamri et al. 2021
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