ERBB2 c.205G>T ;(p.A69S)

Variant ID: 17-37863374-G-T

NM_004448.2(ERBB2):c.205G>T;(p.A69S)

This variant was identified in 1 publication

View GRCh38 version.




Publications:


Personalized ophthalmology.

Clinical Genetics
Porter, L F LF; Black, G C M GC
Publication Date: 2014-07

Variant appearance in text: HER2: A69S
PubMed Link: 24665880
Variant Present in the following documents:
  • Main text
  • cge0086-0001.pdf
View BVdb publication page