Variant ID: 1-55518073-TT-CG

NM_174936.3(PCSK9):c.646_647delinsCG;(p.F216R)

This variant was identified in 1 publication

View GRCh38 version.




Publications:


Case-control study on PCSK9 R496W (rs374603772) and D374Y (rs137852912) mutations in Turkish patients with primary dyslipidemia.

Anatolian Journal Of Cardiology
Eroğlu, Zuhal Z; Tetik Vardarlı, Aslı A; Düzgün, Zekeriya Z; Gündüz, Cumhur C; Bozok Çetintaş, Vildan V; Kayıkçıoğlu, Meral M
Publication Date: 2018-05

Variant appearance in text: PCSK9: F216R
PubMed Link: 29724976
Variant Present in the following documents:
  • Main text
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