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/RCV000112111.3/
NM_007294.4(BRCA1):c.3531del (p.Phe1177fs) AND Breast-ovarian cancer, familial 1 - 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.
https://www.ncbi.nlm.nih.gov/clinvar/RCV000496452/
NM_007294.4(BRCA1):c.2126_2127insA (p.Phe709fs) AND Hereditary breast ovarian cancer syndrome -...
ClinVar archives and aggregates information about relationships among variation and human health.