cancervariants / cancervariants/variation-normalization
parsed to copy number endpoints should allow curie or gene as subject
Open
enhancement
priority:low
- Dominant language
- Python
- Stars
- 15
- Forks
- 2
- PR merge metrics
- No merged PRs in 30d
Description
Our collaborators needs only need `sequence location` for the parsed to copy number endpoints, but the `subject` can also be `curie` or `gene`. We should add support for this
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