Bibliome.ai browser hg19
Search
About
Stats
FAQ
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.
Variant-Specific Resource Links:
gnomAD v2.1.1
Mutalizer Name Checker
Google
UCSC Genome Browser
ClinVar
dbSNP
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