NM_004387.4:c.73C>T

HGVS Expressions

  • NG_013340.1:g.5302C>T
  • NM_004387.4:c.73C>T
  • NP_004378.1:p.Arg25Cys
  • NC_000005.10:g.173235011G>A

Associated Genes

NK2 Homeobox 5
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Clinvar Clinical Significance

Benign, Likely Benign, Uncertain Significance

CTGA Clinical Significance

Likely Benign

Variant Type

Substitution

Clinvar

9008

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