VWF c.4630T>G ;(p.Y1544D)

Variant ID: 12-6127954-A-C

NM_000552.3(VWF):c.4630T>G;(p.Y1544D)

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:

N-linked glycan stabilization of the VWF A2 domain.

Blood
Lynch, Christopher J CJ; Lane, David A DA
Publication Date: 2016-03-31

Variant appearance in text: VWF: Y1544D
PubMed Link: 26773038
Variant Present in the following documents:
  • Main text
View BVdb publication page