NM_024921.4:c.986G>A

  1. Home
  2. NM_024921.4:c.986G>A

HGVS Expressions

  • NG_016358.1:g.76555G>A
  • NM_024921.4:c.986G>A
  • NP_079197.3:p.Arg329Gln
  • NC_000023.11:g.85308188C>T

Associated Genes

POF1B Gene
Back to search Result
Clinvar Clinical Significance

Benign, Likely Pathogenic, Uncertain Significance

Variant Type

Substitution

dbSNP

75398746

Clinvar

10794

Contributors

  • Pratibha Nair: 02.04.2020

Edit History

  • Pratibha Nair: 22.11.2022
  • Pratibha Nair: 02.04.2020
Back to search Result
© CAGS 2024. All rights reserved.
© CAGS 2024. All rights reserved.