VWF c.4358T>A ;(p.I1453N)

Variant ID: 12-6128226-A-T

NM_000552.3(VWF):c.4358T>A;(p.I1453N)

This variant was identified in 1 publication

View GRCh38 version.




Publications:


Clinical and laboratory phenotype variability in type 2M von Willebrand disease.

Journal Of Thrombosis And Haemostasis : Jth
Doruelo, A L AL; Haberichter, S L SL; Christopherson, P A PA; Boggio, L N LN; Gupta, S S; Lentz, S R SR; Shapiro, A D AD; Montgomery, R R RR; Flood, V H VH
Publication Date: 2017-08

Variant appearance in text: VWF: I1453N
PubMed Link: 28544236
Variant Present in the following documents:
  • Main text
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