SI c.1075_1077delinsTGA ;(p.R359*)

Variant ID: 3-164777759-GCG-TCA

NM_001041.3(SI):c.1075_1077delinsTGA;(p.R359*)

This variant was identified in 1 publication

View GRCh38 version.




Publications:


Ilio-femoral venous thrombosis with hereditary antithrombin deficiency: a case report of rare thrombotic disease and successful treatment with catheter directed thrombolysis.

European Heart Journal. Case Reports
Miyashita, Hirokazu H; Tobita, Kazuki K; Morishita, Eriko E; Saito, Shigeru S
Publication Date: 2021-02

Variant appearance in text: SI: Arg359Ter
PubMed Link: 33738401
Variant Present in the following documents:
  • ytaa531.pdf
View BVdb publication page