VWF c.3830A>C ;(p.D1277A)

Variant ID: 12-6128754-T-G

NM_000552.3(VWF):c.3830A>C;(p.D1277A)

This variant was identified in 1 publication

View GRCh38 version.




Publications:


Identification of amino acid residues responsible for von Willebrand factor binding to sulfatide by charged-to-alanine-scanning mutagenesis.

International Journal Of Hematology
Nakayama, Takayuki T; Matsushita, Tadashi T; Yamamoto, Koji K; Mutsuga, Noriko N; Kojima, Tetsuhito T; Katsumi, Akira A; Nakao, Norihiko N; Sadler, J Evan JE; Naoe, Tomoki T; Saito, Hidehiko H
Publication Date: 2008-05

Variant appearance in text: VWF: D1277A
PubMed Link: 18369690
Variant Present in the following documents:
  • Main text
  • 12185_2008_Article_65.pdf
View BVdb publication page