VWF c.4417A>G ;(p.M1473V)

Variant ID: 12-6128167-T-C

NM_000552.3(VWF):c.4417A>G;(p.M1473V)

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:

Molecular coevolution of coagulation factor VIII and von Willebrand factor.

Blood Advances
Zakas, Philip M PM; Coyle, Christopher W CW; Brehm, Anja A; Bayer, Marion M; Solecka-Witulska, Barbara B; Radford, Caelan E CE; Brown, Christine C; Nesbitt, Kate K; Dwyer, Courtney C; Kannicht, Christoph C; Spencer, H Trent HT; Gaucher, Eric A EA; Doering, Christopher B CB; Lillicrap, David D
Publication Date: 2021-02-09

Variant appearance in text: VWF: M1473V
PubMed Link: 33560395
Variant Present in the following documents:
  • Main text
View BVdb publication page