NM_001211.6:c.1535A>G

HGVS Expressions

  • NG_016338.1:g.44940A>G
  • NM_001211.6:c.1535A>G
  • NP_001202.5:p.Glu512Gly
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Genomic Location

chr15:40200948

Clinvar Clinical Significance

Uncertain Significance

CTGA Clinical Significance

Uncertain Significance

Variant Type

Substitution

Clinvar

1061723

Epidemiology in the Arab World

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