NM_000432.4(MYL2):c.456C>T (p.Tyr152=) AND MYL2-related disorder
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Aug 24, 2020
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV004535215.1
Allele description [Variation Report for NM_000432.4(MYL2):c.456C>T (p.Tyr152=)]
NM_000432.4(MYL2):c.456C>T (p.Tyr152=)
Condition(s)
- Name:
- MYL2-related disorder
- Synonyms:
- MYL2-Related Disorders; MYL2-related condition; MYL2-related disease
- Identifiers:
Assertion and evidence details
Last Updated: Sep 8, 2024