VWF c.3368C>G ;(p.A1123G)

Variant ID: 12-6132808-G-C

NM_000552.3(VWF):c.3368C>G;(p.A1123G)

This variant was identified in 1 publication

View GRCh38 version.




Publications:


Genetic and Bioinformatic Strategies to Improve Diagnosis in Three Inherited Bleeding Disorders in Bogotá, Colombia.

Genes
Lago, Juliana J; Groot, Helena H; Navas, Diego D; Lago, Paula P; Gamboa, María M; Calderón, Dayana D; Polanía-Villanueva, Diana C DC
Publication Date: 2021-11-18

Variant appearance in text: VWF: 3368C>G; Ala1123Gly
PubMed Link: 34828413
Variant Present in the following documents:
  • Main text
  • genes-12-01807.pdf
View BVdb publication page