Variant ID: 1-55505547-CT-GC

NM_174936.3(PCSK9):c.37_38delinsGC;(p.L13A)

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:

Atherosclerosis.

Arteriosclerosis, Thrombosis, And Vascular Biology
Lu, Hong H; Daugherty, Alan A
Publication Date: 2015-03

Variant appearance in text: PCSK9: L13a
PubMed Link: 25717174
Variant Present in the following documents:
  • Main text
View BVdb publication page