PC c.1067G>T ;(p.S356I)

Variant ID: 11-66633776-C-A

NM_001040716.1(PC):c.1067G>T;(p.S356I)

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:

Laboratory Limitations of Excluding Hereditary Protein C Deficiency by Chromogenic Assay: Discrepancies of Phenotype and Genotype.

Clinical And Applied Thrombosis/Hemostasis : Official Journal Of The International Academy Of Clinical And Applied Thrombosis/Hemostasis
Seidel, Holger H; Haracska, Bianca B; Naumann, Jennifer J; Westhofen, Philipp P; Hass, Moritz Sebastian MS; Kruppenbacher, Johannes Philipp JP
Publication Date: 2020

Variant appearance in text: PC: 1067G>T
PubMed Link: 32309994
Variant Present in the following documents:
  • Main text
  • 10.1177_1076029620912028.pdf
View BVdb publication page