PRNP c.635A>G ;(p.Q212R)

Variant ID: 20-4680501-A-G

NM_000311.3(PRNP):c.635A>G;(p.Q212R)

This variant was identified in 1 publication

View GRCh38 version.




Publications:


Predictive testing for inherited prion disease: report of 22 years experience.

European Journal Of Human Genetics : Ejhg
Owen, Jane J; Beck, Jon J; Campbell, Tracy T; Adamson, Gary G; Gorham, Michele M; Thompson, Andrew A; Smithson, Sarah S; Rosser, Elizabeth E; Rudge, Peter P; Collinge, John J; Mead, Simon S
Publication Date: 2014-12

Variant appearance in text: PRNP: 635A>G
PubMed Link: 24713662
Variant Present in the following documents:
  • Main text
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