RET c.42del ;(p.L15Cfs*8)

Variant ID: 10-43572748-TG-T

NM_020975.4(RET):c.42del;(p.L15Cfs*8)

This variant was identified in 1 publication

View GRCh38 version.




Publications:


Molecular genetics of syndromic and non-syndromic forms of parathyroid carcinoma.

Human Mutation
Cardoso, Luís L; Stevenson, Mark M; Thakker, Rajesh V RV
Publication Date: 2017-12

Variant appearance in text: RET: 42del
PubMed Link: 28881068
Variant Present in the following documents:
  • Main text
  • HUMU-38-1621.pdf
View BVdb publication page