RET c.*1046G>C

Variant ID: 10-43624763-G-C

NM_020975.4(RET):c.*1046G>C

This variant was identified in 1 publication

View GRCh38 version.




Publications:


RET variants and haplotype analysis in a cohort of Czech patients with Hirschsprung disease.

Plos One
Vaclavikova, Eliska E; Dvorakova, Sarka S; Skaba, Richard R; Pos, Lucie L; Sykorova, Vlasta V; Halkova, Tereza T; Vcelak, Josef J; Bendlova, Bela B
Publication Date: 2014

Variant appearance in text: rs143948954
PubMed Link: 24897126
Variant Present in the following documents:
  • Main text
  • pone.0098957.pdf
View BVdb publication page