RET c.2859T>A ;(p.P953=)

Variant ID: 10-43619176-T-A

NM_020975.4(RET):c.2859T>A;(p.P953=)

This variant was identified in 1 publication

View GRCh38 version.



Variant-Specific Resource Links:
gnomAD v2.1.1
Mutalizer Name Checker
Google
UCSC Genome Browser
ClinVar
dbSNP

Publications:

A novel study of copy number variations in Hirschsprung disease using the multiple ligation-dependent probe amplification (MLPA) technique.

Bmc Medical Genetics
Núñez-Torres, Rocío R; Fernández, Raquel M RM; López-Alonso, Manuel M; Antiñolo, Guillermo G; Borrego, Salud S
Publication Date: 2009-11-19

Variant appearance in text: RET: 2859T>A
PubMed Link: 19925665
Variant Present in the following documents:
  • Main text
  • 1471-2350-10-119.pdf
View BVdb publication page