NM_000120.4:c.1040G>C

HGVS Expressions

  • NG_009776.1:g.37379G>C
  • NM_000120.4:c.1040G>C
  • NP_000111.1:p.Arg347Thr
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Genomic Location

chr1:225842474

CTGA Clinical Significance

Uncertain Significance

Variant Type

Substitution

Epidemiology in the Arab World

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