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VWF c.7669T>A ;(p.C2557S)
Variant ID: 12-6078437-A-T
NM_000552.3(
VWF
):c.7669T>A;(p.C2557S)
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:
The role of exon 45 and 16 in the pathogenesis of Von Willebrand disease in Iranian Patients.
Iranian Journal Of Pediatric Hematology And Oncology
Nasiri, M M; Galehdari, H H; Darbouy, M M; Yavarian, M M; Keikhaee, B B
Publication Date: 2012
Variant appearance in text: VWF: C2557S
PubMed Link:
24575258
Variant Present in the following documents:
Main text
ijpho-2-164.pdf
View BVdb publication page