Bibliome.ai browser hg19
Search
About
Stats
FAQ
HR c.2548G>A ;(p.E850K)
Variant ID: 8-21978291-C-T
NM_005144.4(
HR
):c.2548G>A;(p.E850K)
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:
Abstracts : 31 st European Congress of Pathology.
Virchows Archiv : An International Journal Of Pathology
Publication Date: 2019-09
Variant appearance in text: HR: 2548G>A
PubMed Link:
31440833
Variant Present in the following documents:
Main text
View BVdb publication page