NM_001304480.1:c.1229T>C

HGVS Expressions

  • NG_008626.2:g.207689T>C
  • NM_001304480.1:c.1229T>C
  • NP_001291409.1:p.Met410Thr
  • NC_000012.12:g.32602217T>C
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Clinvar Clinical Significance

Pathogenic, Uncertain Significance

Variant Type

Substitution

Clinvar

1015

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