NM_000302.4:c.955C>T

HGVS Expressions

  • NG_008159.1:g.28939C>T
  • NM_000302.4:c.955C>T
  • NP_001303249.1:p.Arg366Ter
  • NC_000001.11:g.11958627C>T
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Clinvar Clinical Significance

Pathogenic

CTGA Clinical Significance

Pathogenic

Variant Type

Substitution

Clinvar

14364

Epidemiology in the Arab World

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