Software Development
ClinVar Database
Query NCBI ClinVar for variant clinical significance. Search by gene/position, interpret pathogenicity classifications, access via E-utilities API or FTP, annotate VCFs, for genomic medicine.
- Publisher / source
- davila7/claude-code-templates (found on skills.sh)
- Upstream record
- davila7/claude-code-templates
- Version
- Version 3
- Published
- Publication review
- Approved for publication · recorded passed scan 2026-11-02
- Content fingerprint
de761385bfdeb1674d7a7613d4d0eaf444ae3a47d897910e96760feceb0c1c7d