HR c.295T>G ;(p.W99G)

Variant ID: 8-21986389-A-C

NM_005144.4(HR):c.295T>G;(p.W99G)

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:

Abstracts of the 53rd ESPN Annual Meeting, Amsterdam, The Netherlands, September 2021.

Pediatric Nephrology (Berlin, Germany)
Publication Date: 2021-08-25

Variant appearance in text: HR: 295T>G; Trp99Gly
PubMed Link: 34432141
Variant Present in the following documents:
  • 467_2021_Article_5210.pdf
View BVdb publication page