NM_000363.5(TNNI3):c.586G>A (p.Asp196Asn) AND Primary familial hypertrophic cardiomyopathy
- Germline classification:
- Likely pathogenic (1 submission)
- Last evaluated:
- Jun 1, 2014
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000148897.6
Allele description [Variation Report for NM_000363.5(TNNI3):c.586G>A (p.Asp196Asn)]
NM_000363.5(TNNI3):c.586G>A (p.Asp196Asn)
Condition(s)
Assertion and evidence details
Last Updated: May 12, 2024