VWF c.6123C>A ;(p.N2041K)

Variant ID: 12-6103714-G-T

NM_000552.3(VWF):c.6123C>A;(p.N2041K)

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: 6123C>A
PubMed Link: 34272389
Variant Present in the following documents:
  • 41525_2021_228_MOESM1_ESM.pdf
View BVdb publication page