APP c.1732G>C ;(p.A578P)

Variant ID: 21-27284230-C-G

NM_000484.3(APP):c.1732G>C;(p.A578P)

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:

Analyses Mutations in GSN, CST3, TTR, and ITM2B Genes in Chinese Patients With Alzheimer's Disease.

Frontiers In Aging Neuroscience
Jiang, Yaling Y; Jiao, Bin B; Liao, Xinxin X; Xiao, Xuewen X; Liu, Xixi X; Shen, Lu L
Publication Date: 2020

Variant appearance in text: APP: Ala578Pro
PubMed Link: 33192475
Variant Present in the following documents:
  • fnagi-12-581524.pdf
View BVdb publication page