NM_138450.6:c.446G>A

HGVS Expressions

  • NG_021342.1:g.7595G>A
  • NM_138450.6:c.446G>A
  • NP_612459.1:p.Trp149Ter
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Genomic Location

chr13:49630893

Clinvar Clinical Significance

Benign

CTGA Clinical Significance

Uncertain Significance

Variant Type

Substitution

Clinvar

769852

Epidemiology in the Arab World

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