NM_000257.4(MYH7):c.4909G>A (p.Ala1637Thr) AND Primary familial hypertrophic cardiomyopathy
- Germline classification:
- Uncertain significance (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:
- RCV000148696.3
Allele description [Variation Report for NM_000257.4(MYH7):c.4909G>A (p.Ala1637Thr)]
NM_000257.4(MYH7):c.4909G>A (p.Ala1637Thr)
Condition(s)
Assertion and evidence details
Last Updated: Aug 18, 2024