Selecting a Variant
SOP Section 5.1
Begin variant curation
Select “New Variant Curation” in the top right of the interface.
Enter the Variant ID using either the ClinVar Variation ID or the ClinGen Allele Registry ID; please note the Allele Registry allows for novel variants to be registered by users.
Click "Retrieve" and confirm that it is the correct variant.
Then select "View Evidence" to enter Evidence View.

You will now enter Evidence View.
Last updated