ClinMAVE
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资源简介：
ClinMAVE is a manually curated database that integrates multiplexed assays of variant effect for the clinical interpretation of human coding variants. It provides standardized variant annotations, detailed experimental context, functional classifications, cross-assay comparisons and ACMG/AMP-aligned evidence grading, together with ClinVar, gnomAD, TCGA and computational prediction annotations.
创建时间：
2026-07-10
