ERBB2 c.1190T>C ;(p.L397P)

Variant ID: 17-37871580-T-C

NM_004448.2(ERBB2):c.1190T>C;(p.L397P)

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:

Genetic heterogeneity in hepatocellular carcinoma and paired bone metastasis revealed by next-generation sequencing.

International Journal Of Clinical And Experimental Pathology
Jin, Ketao K; Lan, Huanrong H; Wang, Xuanwei X; Lv, Jieqing J
Publication Date: 2017

Variant appearance in text: ERBB2: 1190T>C; Leu397Pro
PubMed Link: 31966388
Variant Present in the following documents:
  • Main text
View BVdb publication page