TG c.872dup ;(p.S292Lfs*11)

Variant ID: 8-133894839-A-AT

NM_003235.4(TG):c.872dup;(p.S292Lfs*11)

This variant was identified in 1 publication

View GRCh38 version.




Publications:


Diagnosis, Phenotype, and Molecular Genetics of Congenital Analbuminemia.

Frontiers In Genetics
Minchiotti, Lorenzo L; Caridi, Gianluca G; Campagnoli, Monica M; Lugani, Francesca F; Galliano, Monica M; Kragh-Hansen, Ulrich U
Publication Date: 2019

Variant appearance in text: TG: 872dup
PubMed Link: 31057599
Variant Present in the following documents:
  • Main text
  • fgene-10-00336.pdf
View BVdb publication page