TLN2 c.4009C>G ;(p.L1337V)

Variant ID: 15-63032952-C-G

NM_015059.2(TLN2):c.4009C>G;(p.L1337V)

This variant was identified in 1 publication

View GRCh38 version.




Publications:


Whole-exome sequencing studies of nonhereditary (sporadic) parathyroid adenomas.

The Journal Of Clinical Endocrinology And Metabolism
Newey, Paul J PJ; Nesbit, M Andrew MA; Rimmer, Andrew J AJ; Attar, Moustafa M; Head, Rosie T RT; Christie, Paul T PT; Gorvin, Caroline M CM; Stechman, Michael M; Gregory, Lorna L; Mihai, Radu R; Sadler, Greg G; McVean, Gil G; Buck, David D; Thakker, Rajesh V RV
Publication Date: 2012-10

Variant appearance in text: TLN2: L1337V
PubMed Link: 22855342
Variant Present in the following documents:
  • Main text
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