VWF c.874+5G>A

Variant ID: 12-6184496-C-T

NM_000552.3(VWF):c.874+5G>A

This variant was identified in 1 publication

View GRCh38 version.




Publications:


The genetics of Canadian type 3 von Willebrand disease: further evidence for co-dominant inheritance of mutant alleles.

Journal Of Thrombosis And Haemostasis : Jth
Bowman, M M; Tuttle, A A; Notley, C C; Brown, C C; Tinlin, S S; Deforest, M M; Leggo, J J; Blanchette, V S VS; Lillicrap, D D; James, P P; ,
Publication Date: 2013-03

Variant appearance in text: VWF: 874+5G>A
PubMed Link: 23311757
Variant Present in the following documents:
  • Main text
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