NM_000258.3(MYL3):c.274G>A (p.Val92Met) AND Cardiomyopathy
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Dec 18, 2020
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000770181.3
Allele description [Variation Report for NM_000258.3(MYL3):c.274G>A (p.Val92Met)]
NM_000258.3(MYL3):c.274G>A (p.Val92Met)
Condition(s)
- Name:
- Cardiomyopathy (CMYO)
- Synonyms:
- Cardiomyopathies
- Identifiers:
- MONDO: MONDO:0004994; MedGen: C0878544; Human Phenotype Ontology: HP:0001638
-
Homo sapiens T cell leukemia translocation altered (TCTA), mRNA
Homo sapiens T cell leukemia translocation altered (TCTA), mRNAgi|2028695540|ref|NM_022171.3|Nucleotide
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See more...Assertion and evidence details
Last Updated: Sep 29, 2024