Nouakchott NM_000517.6:c.344C>T

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  2. Nouakchott NM_000517.6:c.344C>T

HGVS Expressions

  • NG_059271.1:g.5669C>T
  • NM_000517.6:c.344C>T
  • NP_000508.1:p.Pro115Leu

Associated Genes

Hemoglobin--Alpha Locus 2
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Genomic Location

chr16:173515

Clinvar Clinical Significance

Likely Benign, Uncertain Significance

Variant Type

Substitution

dbSNP

267607269

Clinvar

439115

Contributors

  • Sayeeda Hana: 25.11.2020

Edit History

  • Sayeeda Hana: 29.11.2020
  • Sayeeda Hana: 25.11.2020
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© CAGS 2024. All rights reserved.
© CAGS 2024. All rights reserved.