VWF c.905_906insCAACAG ;(p.Y301_R302insSN)

Variant ID: 12-6182876-C-CCTGTTG

NM_000552.3(VWF):c.905_906insCAACAG;(p.Y301_R302insSN)

This variant was identified in 1 publication

View GRCh38 version.




Publications:


Genetic heterogeneity in a large cohort of Indian type 3 von Willebrand disease patients.

Plos One
Kasatkar, Priyanka P; Shetty, Shrimati S; Ghosh, Kanjaksha K
Publication Date: 2014

Variant appearance in text: VWF: E300_R302insSN
PubMed Link: 24675615
Variant Present in the following documents:
  • Main text
  • pone.0092575.pdf
View BVdb publication page