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VWF c.4952T>G ;(p.I1651S)
Variant ID: 12-6127632-A-C
NM_000552.3(
VWF
):c.4952T>G;(p.I1651S)
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: I1651S
PubMed Link:
25564400
Variant Present in the following documents:
Main text
View BVdb publication page