VWF c.1159_1160delinsCC ;(p.E387P)

Variant ID: 12-6174436-TC-GG

NM_000552.3(VWF):c.1159_1160delinsCC;(p.E387P)

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:

Rare Defects: Looking at the Dark Face of the Thrombosis.

International Journal Of Environmental Research And Public Health
D'Andrea, Giovanna G; Margaglione, Maurizio M
Publication Date: 2021-08-30

Variant appearance in text: VWF: E387P
PubMed Link: 34501736
Variant Present in the following documents:
  • Main text
  • ijerph-18-09146.pdf
View BVdb publication page