NM_000540.3(RYR1):c.4377C>T (p.His1459=) AND RYR1-Related Disorders
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Aug 2, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000919440.7
Allele description [Variation Report for NM_000540.3(RYR1):c.4377C>T (p.His1459=)]
NM_000540.3(RYR1):c.4377C>T (p.His1459=)
Condition(s)
- Name:
- RYR1-Related Disorders
- Identifiers:
- MedGen: CN239331
Assertion and evidence details
Last Updated: Apr 20, 2024