01Discover available OpenCRAVAT annotators and inspect their output schemas
02Annotate genomic variants using GRCh38 coordinates, dbSNP rsID, or ClinGen Allele Registry ID
03Support variant annotation via HGVS (g./c./p.) notations
04Convert protein missense notations (e.g., BRAF V600E) into GRCh38 genomic HGVS changes
05Deployable as a Cloudflare Worker or runnable locally for flexible access
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