SLCO1B1 c.680G>C ;(p.G227A)

Variant ID: 12-21331907-G-C

NM_006446.4(SLCO1B1):c.680G>C;(p.G227A)

This variant was identified in 1 publication

View GRCh38 version.




Publications:


Genetic variants associated with gastrointestinal symptoms in Fabry disease.

Oncotarget
Di Martino, Maria Teresa MT; Scionti, Francesca F; Sestito, Simona S; Nicoletti, Angela A; Arbitrio, Mariamena M; Hiram Guzzi, Pietro P; Talarico, Valentina V; Altomare, Federica F; Sanseviero, Maria Teresa MT; Agapito, Giuseppe G; Pisani, Antonio A; Riccio, Eleonora E; Borrelli, Osvaldo O; Concolino, Daniela D; Pensabene, Licia L
Publication Date: 2016-12-27

Variant appearance in text: SLCO1B1: 680G>C
PubMed Link: 27825144
Variant Present in the following documents:
  • Main text
View BVdb publication page