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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