NM_000257.4(MYH7):c.2692C>T (p.Leu898=) AND Hypertrophic cardiomyopathy 1
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Jan 13, 2018
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000315717.12
Allele description [Variation Report for NM_000257.4(MYH7):c.2692C>T (p.Leu898=)]
NM_000257.4(MYH7):c.2692C>T (p.Leu898=)
Condition(s)
Assertion and evidence details
Last Updated: Oct 13, 2024