NM_002524.5:c.182A>G

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HGVS Expressions

  • NG_007572.1:g.7987A>G
  • NM_002524.5:c.182A>G
  • NP_002515.1:p.Gln61Arg
  • NC_000001.11:g.114713908T>C

Associated Genes

NRAS Protooncogene, GTPase
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Clinvar Clinical Significance

Likely Pathogenic, Pathogenic

Variant Type

Substitution

dbSNP

11554290

Clinvar

13900

Contributors

  • Pratibha Nair: 09.05.2021

Edit History

  • Pratibha Nair: 09.05.2021
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© CAGS 2024. All rights reserved.
© CAGS 2024. All rights reserved.