CALR c.1008G>T ;(p.E336D)

Variant ID: 19-13054398-G-T

NM_004343.3(CALR):c.1008G>T;(p.E336D)

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:

Understanding protein structural changes for oncogenic missense variants.

Heliyon
Hernandez, Rolando R; Facelli, Julio C JC
Publication Date: 2021-01

Variant appearance in text: CALR: 1008G>T; Glu336Asp
PubMed Link: 33553733
Variant Present in the following documents:
  • Main text
View BVdb publication page