NF1 c.31_33del ;(p.Q11del)

Variant ID: 17-29422358-CCAG-C

NM_001042492.2(NF1):c.31_33del;(p.Q11del)

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:

Disorders of the genome architecture: a review.

Genomic Medicine
Kumar, Dhavendra D
Publication Date: 2008-12

Variant appearance in text: NF1: q11del
PubMed Link: 19277903
Variant Present in the following documents:
  • Main text
View BVdb publication page