PC c.1192_1194delinsTGT ;(p.R398C)

Variant ID: 11-66631419-CCG-ACA

NM_001040716.1(PC):c.1192_1194delinsTGT;(p.R398C)

This variant was identified in 1 publication

View GRCh38 version.




Publications:


[Clinical phenotype and gene mutation analysis of 12 patients with hereditary protein C deficiency in different families].

Zhonghua Xue Ye Xue Za Zhi = Zhonghua Xueyexue Zazhi
Xu, Q Y QY; Yang, L L LL; Xie, H X HX; Jin, Y H YH; Li, X L XL; Zhou, X X XX; Liu, M N MN; Wang, M S MS
Publication Date: 2022-01-14

Variant appearance in text: PC: Arg398Cys
PubMed Link: 35231991
Variant Present in the following documents:
  • Main text
  • cjh-43-01-035.pdf
View BVdb publication page