MSH2 c.2196T>C ;(p.T732=)

Variant ID: 2-47703696-T-C

NM_000251.2(MSH2):c.2196T>C;(p.T732=)

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:

Advances in the study of Lynch syndrome in China.

World Journal Of Gastroenterology
Lu, Jun-Yu JY; Sheng, Jian-Qiu JQ
Publication Date: 2015-06-14

Variant appearance in text: MSH2: 2196T>C
PubMed Link: 26078562
Variant Present in the following documents:
  • Main text
View BVdb publication page