PC c.795_796insA ;(p.S266Ifs*35)

Variant ID: 11-66637880-A-AT

NM_001040716.1(PC):c.795_796insA;(p.S266Ifs*35)

This variant was identified in 1 publication

View GRCh38 version.




Publications:


Genotypic and phenotypic character of Chinese neonates with congenital protein C deficiency: a case report and literature review.

Thrombosis Journal
Li, Xiaoying X; Li, Xiaoyan X; Li, Xiao X; Zhuang, Yuanhua Y; Kang, Lili L; Ju, Xiuli X
Publication Date: 2019

Variant appearance in text: PC: 795_796insA
PubMed Link: 31592240
Variant Present in the following documents:
  • Main text
  • 12959_2019_Article_208.pdf
View BVdb publication page