NM_000256.3(MYBPC3):c.961G>A (p.Val321Met) AND Primary familial hypertrophic cardiomyopathy
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Sep 6, 2016
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000627153.4
Allele description [Variation Report for NM_000256.3(MYBPC3):c.961G>A (p.Val321Met)]
NM_000256.3(MYBPC3):c.961G>A (p.Val321Met)
Condition(s)
Assertion and evidence details
Last Updated: Oct 13, 2024