NM_001085427.2:c.585G>T

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HGVS Expressions

  • NG_009260.2:g.6247G>T
  • NM_001085427.2:c.585G>T
  • NP_001078896.2:p.Trp195Cys
  • NC_000022.11:g.50626933C>A

Associated Genes

Arylsulfatase A
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Clinvar Clinical Significance

Benign

Variant Type

Substitution

dbSNP

6151415

Clinvar

93125

Contributors

  • Pratibha Nair: 24.04.2018

Edit History

  • Pratibha Nair: 12.10.2022
  • Pratibha Nair: 07.11.2018
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© CAGS 2024. All rights reserved.
© CAGS 2024. All rights reserved.