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VWF c.3961T>G ;(p.Y1321D)
Variant ID: 12-6128623-A-C
NM_000552.3(
VWF
):c.3961T>G;(p.Y1321D)
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:
Laboratory testing for von Willebrand disease: toward a mechanism-based classification.
Clinics In Laboratory Medicine
Torres, Richard R; Fedoriw, Yuri Y
Publication Date: 2009-06
Variant appearance in text: VWF: Y1321D
PubMed Link:
19665675
Variant Present in the following documents:
Main text
View BVdb publication page