VWF c.7126C>T ;(p.P2376S)

Variant ID: 12-6091113-G-A

NM_000552.3(VWF):c.7126C>T;(p.P2376S)

This variant was identified in 1 publication

View GRCh38 version.




Publications:


Molecular classification of blood and bleeding disorder genes.

Npj Genomic Medicine
Baz, Batoul B; Abouelhoda, Mohamed M; Owaidah, Tarek T; Dasouki, Majed M; Monies, Dorota D; Al Tassan, Nada N
Publication Date: 2021-07-16

Variant appearance in text: VWF: 7126C>T; Pro2376Ser; rs775107211
PubMed Link: 34272389
Variant Present in the following documents:
  • 41525_2021_228_MOESM1_ESM.pdf
View BVdb publication page