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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.
Variant-Specific Resource Links:
gnomAD v2.1.1
Mutalizer Name Checker
Google
UCSC Genome Browser
ClinVar
dbSNP
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