NM_173483.3:c.1303C>T

HGVS Expressions

  • NG_007987.1:g.45646C>T
  • NM_173483.3:c.1303C>T
  • NM_173483.3:c.1303C>T
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Genomic Location

chr19:15549170

Clinvar Clinical Significance

Pathogenic

CTGA Clinical Significance

Pathogenic

Variant Type

Substitution

Clinvar

909

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