NM_015080.4:c.1718G>A

HGVS Expressions

  • NG_047107.1:g.60859G>A
  • NM_015080.4:c.1718G>A
  • NP_055895.1:p.Gly573Asp
  • NC_000011.10:g.64667330C>T

Associated Genes

Neurexin II
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CTGA Clinical Significance

Uncertain Significance

Variant Type

Substitution

Epidemiology in the Arab World

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