Bibliome.ai browser hg19
Search
About
Stats
FAQ
TG c.872dup ;(p.S292Lfs*11)
Variant ID: 8-133894839-A-AT
NM_003235.4(
TG
):c.872dup;(p.S292Lfs*11)
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:
Diagnosis, Phenotype, and Molecular Genetics of Congenital Analbuminemia.
Frontiers In Genetics
Minchiotti, Lorenzo L; Caridi, Gianluca G; Campagnoli, Monica M; Lugani, Francesca F; Galliano, Monica M; Kragh-Hansen, Ulrich U
Publication Date: 2019
Variant appearance in text: TG: 872dup
PubMed Link:
31057599
Variant Present in the following documents:
Main text
fgene-10-00336.pdf
View BVdb publication page