APP c.1655C>A ;(p.P552H)

Variant ID: 21-27326936-G-T

NM_000484.3(APP):c.1655C>A;(p.P552H)

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: P552H
PubMed Link: 31011701
Variant Present in the following documents:
  • Main text
  • RTH2-3-173.pdf
View BVdb publication page