NM_001267550.2(TTN):c.79700A>G (p.Asn26567Ser) AND Hypertrophic cardiomyopathy
- Germline classification:
- Benign (1 submission)
- Last evaluated:
- May 8, 2018
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000852808.2
Allele description [Variation Report for NM_001267550.2(TTN):c.79700A>G (p.Asn26567Ser)]
NM_001267550.2(TTN):c.79700A>G (p.Asn26567Ser)
Condition(s)
- Name:
- Hypertrophic cardiomyopathy
- Synonyms:
- HYPERTROPHIC MYOCARDIOPATHY
- Identifiers:
- MONDO: MONDO:0005045; MeSH: D002312; MedGen: C0007194; Human Phenotype Ontology: HP:0001639
Assertion and evidence details
Last Updated: Oct 8, 2024