NM_024734.4:c.730C>T

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HGVS Expressions

  • NM_024734.4:c.730C>T
  • NP_079010.2:p.Arg244Ter
  • NC_000014.9:g.95210758G>A

Associated Genes

Calmin
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CTGA Clinical Significance

Uncertain Significance

Variant Type

Substitution

dbSNP

765515059

Epidemiology in the Arab World

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Subject IDCountry of OriginAllele CountAllele FrequencyCTGA Clinical Significance Condition(s)ReferenceRemarks
613192.1Egypt2Uncertain SignificanceReuter et al. 2017 Authors classified the CLMN gene variant...
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Contributors

  • Sayeeda Hana: 15.10.2024

Edit History

  • Sayeeda Hana: 15.10.2024
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© CAGS 2024. All rights reserved.
© CAGS 2024. All rights reserved.