APP c.68A>C ;(p.D23A)

Variant ID: 21-27484453-T-G

NM_000484.3(APP):c.68A>C;(p.D23A)

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:

Cerebral amyloid angiopathy-linked β-amyloid mutations promote cerebral fibrin deposits via increased binding affinity for fibrinogen.

Proceedings Of The National Academy Of Sciences Of The United States Of America
Cajamarca, Steven A SA; Norris, Erin H EH; van der Weerd, Louise L; Strickland, Sidney S; Ahn, Hyung Jin HJ
Publication Date: 2020-06-23

Variant appearance in text: APP: D23A
PubMed Link: 32518112
Variant Present in the following documents:
  • Main text
View BVdb publication page