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ERBB2 c.1803C>T ;(p.P601=)
Variant ID: 17-37873638-C-T
NM_004448.2(
ERBB2
):c.1803C>T;(p.P601=)
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: 1803C>T
PubMed Link:
31966388
Variant Present in the following documents:
Main text
View BVdb publication page