VWF c.4982C>G ;(p.A1661G)

Variant ID: 12-6127602-G-C

NM_000552.3(VWF):c.4982C>G;(p.A1661G)

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:

Structural basis of type 2A von Willebrand disease investigated by molecular dynamics simulations and experiments.

Plos One
Interlandi, Gianluca G; Ling, Minhua M; Tu, An Yue AY; Chung, Dominic W DW; Thomas, Wendy E WE
Publication Date: 2012

Variant appearance in text: VWF: A1661G
PubMed Link: 23110044
Variant Present in the following documents:
  • Main text
  • pone.0045207.pdf
View BVdb publication page