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VWF c.7526A>G ;(p.D2509G)
Variant ID: 12-6080787-T-C
NM_000552.3(
VWF
):c.7526A>G;(p.D2509G)
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:
Von Willebrand Factor Abnormalities Studied in the Mouse Model: What We Learned about VWF Functions.
Mediterranean Journal Of Hematology And Infectious Diseases
Casari, Caterina C; Lenting, Peter J PJ; Christophe, Olivier D OD; Denis, Cécile V CV
Publication Date: 2013
Variant appearance in text: VWF: D2509G
PubMed Link:
23936618
Variant Present in the following documents:
Main text
mjhid-5-1-e2013047.pdf
View BVdb publication page