HR c.1802G>C ;(p.S601T)

Variant ID: 8-21981275-C-G

NM_005144.4(HR):c.1802G>C;(p.S601T)

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: 1802G>C
PubMed Link: 34432141
Variant Present in the following documents:
  • 467_2021_Article_5210.pdf
View BVdb publication page