RET c.1488C>T ;(p.A496=)

Variant ID: 10-43606879-C-T

NM_020975.4(RET):c.1488C>T;(p.A496=)

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:

Rapid mutation screening for HRPT2 and MEN1 mutations associated with familial and sporadic primary hyperparathyroidism.

The Journal Of Molecular Diagnostics : Jmd
Howell, Viive M VM; Cardinal, John W JW; Richardson, Anne-Louise AL; Gimm, Oliver O; Robinson, Bruce G BG; Marsh, Deborah J DJ
Publication Date: 2006-11

Variant appearance in text: RET: 1488C>T
PubMed Link: 17065424
Variant Present in the following documents:
  • Main text
View BVdb publication page