NM_001267039.1:c.752del

HGVS Expressions

  • NG_032779.1:g.15320del
  • NM_001267039.1:c.752del
  • NP_001253968.1:p.Ser251ThrfsTer8
  • NC_000004.12:g.112647283del
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CTGA Clinical Significance

Likely Pathogenic

Variant Type

Deletion

Epidemiology in the Arab World

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