SI c.3419C>T ;(p.P1140L)

Variant ID: 3-164737394-G-A

NM_001041.3(SI):c.3419C>T;(p.P1140L)

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 genetics of Wilson disease.

Handbook Of Clinical Neurology
Chang, Irene J IJ; Hahn, Si Houn SH
Publication Date: 2017

Variant appearance in text: SI: 3419C>T
PubMed Link: 28433102
Variant Present in the following documents:
  • Main text
View BVdb publication page