NM_181458.4:c.449C>A

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HGVS Expressions

  • NG_011632.1:g.8452C>A
  • NM_181458.4:c.449C>A
  • NP_852123.1:p.Ser150Ter
  • NC_000002.12:g.222295530G>T

Associated Genes

Paired Box Gene 3
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CTGA Clinical Significance

Likely Pathogenic

Variant Type

Substitution

Epidemiology in the Arab World

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Contributors

  • Asha Deepthi: 13.12.2024

Edit History

  • Asha Deepthi: 22.01.2025
  • Asha Deepthi: 13.12.2024
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© CAGS 2025. All rights reserved.
© CAGS 2025. All rights reserved.