Bibliome.ai browser hg19
Search
About
Stats
FAQ
CALR c.894G>A ;(p.E298=)
Variant ID: 19-13051635-G-A
NM_004343.3(
CALR
):c.894G>A;(p.E298=)
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:
Genetic polymorphism G894T and the prognosis of heart failure outpatients.
Arquivos Brasileiros De Cardiologia
Tardin, Oziel Marcio Araujo OM; Pereira, Sabrina Bernardez SB; Velloso, Monica Wanderley Monçores MW; Balieiro, Henrique Miller HM; Costa, Bruno B; Alves, Thiago Oliveira e TO; Giro, Camila C; Pessoa, Leandro Pontes LP; Ribeiro, Georgina Severo GS; Mesquita, Evandro Tinoco ET
Publication Date: 2013-10
Variant appearance in text: CRT: Glu298Glu
PubMed Link:
23949326
Variant Present in the following documents:
Main text
abc-101-04-0352.pdf
View BVdb publication page