Variant ID: 1-55527189-G-T

NM_174936.3(PCSK9):c.1823G>T;(p.C608F)

This variant was identified in 1 publication

View GRCh38 version.




Publications:


Patterns and tempo of PCSK9 pseudogenizations suggest an ancient divergence in mammalian cholesterol homeostasis mechanisms.

Genetica
van Asch, Barbara B; Teixeira da Costa, Luís Filipe LF
Publication Date: 2021-02

Variant appearance in text: PCSK9: C608F
PubMed Link: 33515402
Variant Present in the following documents:
  • Main text
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