LRP1 c.1402A>T ;(p.R468W)

Variant ID: 12-57550051-A-T

NM_002332.2(LRP1):c.1402A>T;(p.R468W)

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:

Regulation of PCSK9 Expression and Function: Mechanisms and Therapeutic Implications.

Frontiers In Cardiovascular Medicine
Xia, Xiao-Dan XD; Peng, Zhong-Sheng ZS; Gu, Hong-Mei HM; Wang, Maggie M; Wang, Gui-Qing GQ; Zhang, Da-Wei DW
Publication Date: 2021

Variant appearance in text: LRP1: R468W
PubMed Link: 34782856
Variant Present in the following documents:
  • Main text
View BVdb publication page