NM_001360016.2:c.1311T>C

HGVS Expressions

  • NG_009015.2:g.20134T>C
  • NM_001360016.2:c.1311T>C
  • NP_001346945.1:p.Tyr437=
  • NC_000023.11:g.154532439A>G
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Clinvar Clinical Significance

Benign

CTGA Clinical Significance

Benign, Likely Benign

Variant Type

Substitution

dbSNP

2230037

Clinvar

470162

Epidemiology in the Arab World

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