VWF c.7332G>A ;(p.W2444*)

Variant ID: 12-6085382-C-T

NM_000552.3(VWF):c.7332G>A;(p.W2444*)

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:

[Mutation analysis of VWF gene in two patients with von Willebrand disease by target sequence capture and high-throughput sequencing technology].

Zhonghua Xue Ye Xue Za Zhi = Zhonghua Xueyexue Zazhi
Feng, Y Y; Mei, S Y SY; Liu, N N; Guo, R X RX
Publication Date: 2018-03-14

Variant appearance in text: VWF: 7332G>A; W2444X
PubMed Link: 29562472
Variant Present in the following documents:
  • Main text
  • cjh-39-03-242.pdf
View BVdb publication page