NM_000129.4:c.103G>T

HGVS Expressions

  • NG_008107.1:g.7130G>T
  • NM_000129.4:c.103G>T
  • NP_000120.2:p.Val35Leu
  • NC_000006.12:g.6318562C>A

Associated Genes

Factor XIII, A1 Subunit
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Clinvar Clinical Significance

Benign, Uncertain Significance

CTGA Clinical Significance

Benign, Uncertain Significance

Variant Type

Substitution

dbSNP

5985

Clinvar

16532

Epidemiology in the Arab World

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