NM_000432.4(MYL2):c.424T>C (p.Phe142Leu) AND Cardiomyopathy
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Dec 8, 2020
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV001526320.2
Allele description [Variation Report for NM_000432.4(MYL2):c.424T>C (p.Phe142Leu)]
NM_000432.4(MYL2):c.424T>C (p.Phe142Leu)
Condition(s)
- Name:
- Cardiomyopathy (CMYO)
- Synonyms:
- Cardiomyopathies
- Identifiers:
- MONDO: MONDO:0004994; MedGen: C0878544; Human Phenotype Ontology: HP:0001638
-
eggc.vipovO (0)
BioProject
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Last Updated: May 7, 2024