NM_001035.3(RYR2):c.726C>T (p.Asp242=) AND Cardiomyopathy
- Germline classification:
- Benign (2 submissions)
- Last evaluated:
- Aug 6, 2018
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000768756.12
Allele description [Variation Report for NM_001035.3(RYR2):c.726C>T (p.Asp242=)]
NM_001035.3(RYR2):c.726C>T (p.Asp242=)
Condition(s)
- Name:
- Cardiomyopathy (CMYO)
- Synonyms:
- Cardiomyopathies
- Identifiers:
- MONDO: MONDO:0004994; MedGen: C0878544; Human Phenotype Ontology: HP:0001638
Assertion and evidence details
Last Updated: Apr 20, 2024