WNK4 c.1442G>A ;(p.G481D)

Variant ID: 17-40937466-G-A

NM_032387.4(WNK4):c.1442G>A;(p.G481D)

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:

The variety of genetic defects explains the phenotypic heterogeneity of Familial Hyperkalemic Hypertension.

Kidney International Reports
Hureaux, Marguerite M; Mazurkiewicz, Stephani S; Boccio, Valerie V; Vargas-Poussou, Rosa R; Jeunemaitre, Xavier X
Publication Date: 2021-10

Variant appearance in text: WNK4: 1442G>A
PubMed Link: 34622103
Variant Present in the following documents:
  • mmc1.pdf
View BVdb publication page