TNFSF11 c.81G>A ;(p.E27=)

Variant ID: 13-43148520-G-A

NM_003701.3(TNFSF11):c.81G>A;(p.E27=)

This variant was identified in 1 publication

View GRCh38 version.




Publications:


Lack of Myosin X Enhances Osteoclastogenesis and Increases Cell Surface Unc5b in Osteoclast-Lineage Cells.

Journal Of Bone And Mineral Research : The Official Journal Of The American Society For Bone And Mineral Research
Wang, Bo B; Pan, Jin-Xiu JX; Yu, Huali H; Xiong, Lei L; Zhao, Kai K; Xiong, Shan S; Guo, Jun-Peng JP; Lin, Sen S; Sun, Dong D; Zhao, Lu L; Guo, Haohan H; Mei, Lin L; Xiong, Wen-Cheng WC
Publication Date: 2019-05

Variant appearance in text: RANKL: E27E
PubMed Link: 30645777
Variant Present in the following documents:
  • Main text
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