RET c.1334C>T ;(p.S445F)

Variant ID: 10-43606725-C-T

NM_020975.4(RET):c.1334C>T;(p.S445F)

This variant was identified in 1 publication

View GRCh38 version.



Variant-Specific Resource Links:
gnomAD v2.1.1
Mutalizer Name Checker
Google
UCSC Genome Browser
ClinVar
dbSNP

Publications:

Genetic and Clinical Profiles of Pheochromocytoma and Paraganglioma: A Single Center Study.

Frontiers In Endocrinology
Ma, Xiaosen X; Li, Ming M; Tong, Anli A; Wang, Fen F; Cui, Yunying Y; Zhang, Xuebin X; Zhang, Yushi Y; Chen, Shi S; Li, Yuxiu Y
Publication Date: 2020

Variant appearance in text: RET: 1334C>T; S445L
PubMed Link: 33362715
Variant Present in the following documents:
  • fendo-11-574662.pdf
View BVdb publication page