APP c.934A>G ;(p.T312A)

Variant ID: 21-27372429-T-C

NM_000484.3(APP):c.934A>G;(p.T312A)

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:

Fibrinogen αC domain: Its importance in physiopathology.

Research And Practice In Thrombosis And Haemostasis
Soria, Jeannette J; Mirshahi, Shahsoltan S; Mirshahi, Sam Qiumars SQ; Varin, Remi R; Pritchard, Linda L LL; Soria, Claudine C; Mirshahi, Massoud M
Publication Date: 2019-04

Variant appearance in text: APP: T312A
PubMed Link: 31011701
Variant Present in the following documents:
  • Main text
  • RTH2-3-173.pdf
View BVdb publication page