NM_001267550.2(TTN):c.63793G>A (p.Asp21265Asn) AND Cardiovascular phenotype
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Sep 23, 2020
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV002453683.9
Allele description [Variation Report for NM_001267550.2(TTN):c.63793G>A (p.Asp21265Asn)]
NM_001267550.2(TTN):c.63793G>A (p.Asp21265Asn)
Condition(s)
- Name:
- Cardiovascular phenotype
- Identifiers:
- MedGen: CN230736
Assertion and evidence details
Last Updated: Nov 30, 2024