NM_000258.3(MYL3):c.466G>T (p.Val156Leu) AND Primary familial hypertrophic cardiomyopathy
- Germline classification:
- Uncertain significance (1 submission)
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000845401.3
Allele description [Variation Report for NM_000258.3(MYL3):c.466G>T (p.Val156Leu)]
NM_000258.3(MYL3):c.466G>T (p.Val156Leu)
Condition(s)
Assertion and evidence details
Last Updated: May 7, 2024