VWF c.1087C>T ;(p.L363F)

Variant ID: 12-6181519-G-A

NM_000552.3(VWF):c.1087C>T;(p.L363F)

This variant was identified in 1 publication

View GRCh38 version.




Publications:


VWF mutations and new sequence variations identified in healthy controls are more frequent in the African-American population.

Blood
Bellissimo, Daniel B DB; Christopherson, Pamela A PA; Flood, Veronica H VH; Gill, Joan Cox JC; Friedman, Kenneth D KD; Haberichter, Sandra L SL; Shapiro, Amy D AD; Abshire, Thomas C TC; Leissinger, Cindy C; Hoots, W Keith WK; Lusher, Jeanne M JM; Ragni, Margaret V MV; Montgomery, Robert R RR
Publication Date: 2012-03-01

Variant appearance in text: VWF: L363F
PubMed Link: 22197721
Variant Present in the following documents:
  • Main text
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