VWF c.4925T>G ;(p.I1642S)

Variant ID: 12-6127659-A-C

NM_000552.3(VWF):c.4925T>G;(p.I1642S)

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:

The role of the ADAMTS13 cysteine-rich domain in VWF binding and proteolysis.

Blood
de Groot, Rens R; Lane, David A DA; Crawley, James T B JT
Publication Date: 2015-03-19

Variant appearance in text: VWF: I1642S
PubMed Link: 25564400
Variant Present in the following documents:
  • Main text
View BVdb publication page