NM_001394783.1:c.554_585del

HGVS Expressions

  • NG_012637.1:g.8315_8346del
  • NM_001394783.1:c.554_585del
  • NP_001381712.1:p.Ser185IlefsTer32
  • NC_000003.12:g.46373456_46373487del
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Clinvar Clinical Significance

Benign, Protective, Risk factor

CTGA Clinical Significance

Uncertain Significance

Variant Type

Deletion

dbSNP

333

Clinvar

8184

Epidemiology in the Arab World

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