NM_000540.3(RYR1):c.7662G>C (p.Leu2554=) AND RYR1-related disorder
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Mar 12, 2020
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV001414349.7
Allele description [Variation Report for NM_000540.3(RYR1):c.7662G>C (p.Leu2554=)]
NM_000540.3(RYR1):c.7662G>C (p.Leu2554=)
Condition(s)
- Name:
- RYR1-related disorder
- Synonyms:
- RYR1-Related Disorders; RYR1-related condition
- Identifiers:
- MedGen: CN239331
Assertion and evidence details
Last Updated: May 19, 2024