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NAGS c.849G>T ;(p.K283N)
Variant ID: 17-42083539-G-T
NM_153006.2(
NAGS
):c.849G>T;(p.K283N)
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:
Clinical characteristics of primary carnitine deficiency: A structured review using a case-by-case approach.
Journal Of Inherited Metabolic Disease
Crefcoeur, Loek L LL; Visser, Gepke G; Ferdinandusse, Sacha S; Wijburg, Frits A FA; Langeveld, Mirjam M; Sjouke, Barbara B
Publication Date: 2022-05
Variant appearance in text: NAGS: 849G>T
PubMed Link:
34997761
Variant Present in the following documents:
Main text
JIMD-45-386.pdf
View BVdb publication page