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