ITGA9 c.38T>C ;(p.L13P)

Variant ID: 3-37493903-T-C

NM_002207.2(ITGA9):c.38T>C;(p.L13P)

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:

Guide to Simulating Complex NMR Probe Circuits.

Concepts In Magnetic Resonance. Part A, Bridging Education And Research
Doty, F David FD
Publication Date: 2018-03

Variant appearance in text: RLC: L13p
PubMed Link: 31178669
Variant Present in the following documents:
  • Main text
View BVdb publication page