ala1708val - Robuta Search

https://www.ncbi.nlm.nih.gov/clinvar/RCV001253393.1/ NM_007294.4(BRCA1):c.5123CT (p.Ala1708Val) AND Deafness, autosomal dominant 13 - ClinVar - NCBI ClinVar archives and aggregates information about relationships among variation and human health. https://www.ncbi.nlm.nih.gov/clinvar/RCV000131166.9/ NM_007294.4(BRCA1):c.5123CT (p.Ala1708Val) AND Hereditary cancer-predisposing syndrome - ClinVar -... ClinVar archives and aggregates information about relationships among variation and human health.