antithrombin III Arg197STOP

Preferred Label : antithrombin III Arg197STOP;

MeSH note : Arg(197) codon replaced by stop codon TGA (R197X); one of two mutations responsible for hereditary type Ia antithrombin III deficiency;

Is substance : O;

Details

Origin ID

C094963;

UMLS CUI

C0300439;

MeSH term(s) associated for indexing
- antithrombin III [MeSH Descriptor]
Record concept(s)
- antithrombin III Arg197STOP [MeSH concept]
Semantic type(s)
- Amino Acid, Peptide, or Protein [UMLS semantic type]

Keyword's position in hierarchy(ies) :

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