APOB c.784A>G ;(p.K262E)

Variant ID: 2-21258490-T-C

NM_000384.2(APOB):c.784A>G;(p.K262E)

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:

Insights into blood lipids from rare variant discovery.

Current Opinion In Genetics & Development
Schmidt, Ellen M EM; Willer, Cristen J CJ
Publication Date: 2015-08

Variant appearance in text: APOB: K262E
PubMed Link: 26241468
Variant Present in the following documents:
  • Main text
View BVdb publication page