NM_024006.6:c.292C>T

HGVS Expressions

  • NG_011564.1:g.8622C>T
  • NM_024006.6:c.292C>T
  • NP_076869.1:p.Arg98Trp
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Genomic Location

chr16:31091334

Clinvar Clinical Significance

Pathogenic

CTGA Clinical Significance

Pathogenic

Variant Type

Substitution

Clinvar

2206

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