NM_000257.4(MYH7):c.77C>T (p.Ala26Val) AND Primary familial hypertrophic cardiomyopathy
- Germline classification:
- Benign (2 submissions)
- Last evaluated:
- Jun 24, 2013
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000148713.13
Allele description [Variation Report for NM_000257.4(MYH7):c.77C>T (p.Ala26Val)]
NM_000257.4(MYH7):c.77C>T (p.Ala26Val)
Condition(s)
Assertion and evidence details
Last Updated: Aug 25, 2024