PKD1 c.7376G>A ;(p.G2459D)

Variant ID: 16-2156512-C-T

NM_001009944.2(PKD1):c.7376G>A;(p.G2459D)

This variant was identified in 1 publication

View GRCh38 version.




Publications:


Strategies in Rapid Genetic Diagnostics of Critically Ill Children: Experiences From a Dutch University Hospital.

Frontiers In Pediatrics
Imafidon, Miriam E ME; Sikkema-Raddatz, Birgit B; Abbott, Kristin M KM; Meems-Veldhuis, Martine T MT; Swertz, Morris A MA; van der Velde, K Joeri KJ; Beunders, Gea G; Bos, Dennis K DK; Knoers, Nine V A M NVAM; Kerstjens-Frederikse, Wilhelmina S WS; van Diemen, Cleo C CC
Publication Date: 2021

Variant appearance in text: PKD1: 7376G>A; Gly2459Asp
PubMed Link: 34136434
Variant Present in the following documents:
  • Main text
  • fped-09-600556.pdf
View BVdb publication page