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