NM_000321.2:c.2247_2248insAA

HGVS Expressions

  • NG_009009.1:g.166287_166288insAA
  • NP_000312.2:p.Asp750fs
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Genomic Location

chr13:48465033-48465034

Clinvar Clinical Significance

Pathogenic

CTGA Clinical Significance

Pathogenic

Variant Type

Insertion

Clinvar

527930

Epidemiology in the Arab World

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