VariantValidator

Validates HGVS sequence descriptions and flawlessly maps transcript/genomic variant data.

What it does

Auto-corrects syntax mistakes and converts genomic VCF descriptions into standardized HGVS format for seamless clinical pipeline integration.

How to use

See https://variantvalidator.org/ for documentation and access.

STRC usage

PARTIAL — Service intermittently unavailable. When working, validates HGVS notation and maps across transcripts.

Connections