TTN c.26863A>G ;(p.I8955V)

Variant ID: 2-179577998-T-C

NM_001267550.1(TTN):c.26863A>G;(p.I8955V)

This variant was identified in 2 publications

View GRCh38 version.




Publications:


Mutation analysis by direct and whole exome sequencing in familial and sporadic tooth agenesis.

International Journal Of Molecular Medicine
Salvi, Alessandro A; Giacopuzzi, Edoardo E; Bardellini, Elena E; Amadori, Francesca F; Ferrari, Lia L; De Petro, Giuseppina G; Borsani, Giuseppe G; Majorana, Alessandra A
Publication Date: 2016-11

Variant appearance in text: TTN: I8955V
PubMed Link: 27665865
Variant Present in the following documents:
  • Main text
  • ijmm-38-05-1338.pdf
View BVdb publication page