NM_001365276.2(TNXB):c.4562C>T (p.Ala1521Val) AND Cardiovascular phenotype
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Jun 15, 2021
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV002334223.3
Allele description [Variation Report for NM_001365276.2(TNXB):c.4562C>T (p.Ala1521Val)]
NM_001365276.2(TNXB):c.4562C>T (p.Ala1521Val)
Condition(s)
- Name:
- Cardiovascular phenotype
- Identifiers:
- MedGen: CN230736
Assertion and evidence details
Last Updated: Sep 29, 2024