NM_005236.3:c.1633G>C

HGVS Expressions

  • NG_011442.1:g.20409G>C
  • NM_005236.3:c.1633G>C
  • NP_005227.1:p.Gly545Arg
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Genomic Location

chr16:13935565

CTGA Clinical Significance

Uncertain Significance

Variant Type

Substitution

Epidemiology in the Arab World

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