NM_032444.4:c.1186C>G

HGVS Expressions

  • NG_028123.1:g.18608C>G
  • NM_032444.4:c.1186C>G
  • NP_115820.2:p.Leu396Val
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Genomic Location

chr16:3597977

CTGA Clinical Significance

Uncertain Significance

Variant Type

Substitution

Clinvar

803201

Epidemiology in the Arab World

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