NM_000426.3:c.3829C>T

HGVS Expressions

  • NG_008678.1:g.437715C>T
  • NM_000426.3:c.3829C>T
  • NP_000417.2:p.Arg1277Ter

Associated Genes

Laminin, Alpha-2
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Genomic Location

chr6:129315855

Clinical Significance

Pathogenic

Variant Type

Substitution

Clinvar

477464

Epidemiology in the Arab World

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Subject IDCountry of OriginAllele CountClinical SignificanceCondition(s)ReferenceRemarks
607855.2Lebanon1PathogenicMuscular Dystrophy, Congenital Merosin-Deficient, 1ANair et al. 2018
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