Variant ID: 1-55512260-C-T

NM_174936.3(PCSK9):c.464C>T;(p.P155L)

This variant was identified in 1 publication

View GRCh38 version.




Publications:


The genetic spectrum of familial hypercholesterolemia in Pakistan.

Clinica Chimica Acta; International Journal Of Clinical Chemistry
Ahmed, Waqas W; Whittall, Ros R; Riaz, Moeen M; Ajmal, Muhammad M; Sadeque, Ahmed A; Ayub, Humaira H; Qamar, Raheel R; Humphries, Steve E SE
Publication Date: 2013-06-05

Variant appearance in text: PCSK9: 464C>T; P155L
PubMed Link: 23535506
Variant Present in the following documents:
  • Main text
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