NM_000257.4(MYH7):c.4908C>T (p.Ala1636=) AND Cardiomyopathy
- Germline classification:
- Likely benign (3 submissions)
- Last evaluated:
- Dec 1, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000769442.15
Allele description [Variation Report for NM_000257.4(MYH7):c.4908C>T (p.Ala1636=)]
NM_000257.4(MYH7):c.4908C>T (p.Ala1636=)
Condition(s)
- Name:
- Cardiomyopathy (CMYO)
- Synonyms:
- Cardiomyopathies
- Identifiers:
- MONDO: MONDO:0004994; MedGen: C0878544; Human Phenotype Ontology: HP:0001638
-
B.cereus bc542a gene
B.cereus bc542a genegi|2462089|emb|Y11171.1|Nucleotide
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See more...Assertion and evidence details
Last Updated: Jun 29, 2024