NM_004006.3:c.5005G>A

HGVS Expressions

  • NG_012232.1:g.979570G>A
  • NM_004006.3:c.5005G>A
  • NP_003997.2:p.Glu1669Lys
  • NC_000023.11:g.32365040C>T

Associated Genes

Dystrophin
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CTGA Clinical Significance

Uncertain Significance

Variant Type

Substitution

Epidemiology in the Arab World

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