Bibliome.ai browser hg19
Search
About
Stats
FAQ
KIT c.1726_1727delinsAA ;(p.L576N)
Variant ID: 4-55593660-CT-AA
NM_000222.2(
KIT
):c.1726_1727delinsAA;(p.L576N)
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:
Results of the UK NEQAS for Molecular Genetics reference sample analysis.
Journal Of Clinical Pathology
Richman, Susan D SD; Fairley, Jennifer J; Hall, Jacqueline A JA; Nataraj, Nakul N; Bhide, Mrudul M; Lau, Aron A; Norman, Kara L KL; Deans, Zandra C ZC
Publication Date: 2018-11
Variant appearance in text: KIT: Leu576Asn
PubMed Link:
30030291
Variant Present in the following documents:
Main text
jclinpath-2018-205277.pdf
View BVdb publication page