NM_175876.4:c.1819_1820del

HGVS Expressions

  • NG_051632.1:g.6946_6947del
  • NM_175876.4:c.1819_1820del
  • NP_787072.2:p.Asp607Ter
  • NC_000001.11:g.231335926_231335927del
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CTGA Clinical Significance

Pathogenic

Variant Type

Deletion

Epidemiology in the Arab World

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