NM_000540.3(RYR1):c.7798C>T (p.Arg2600Cys) AND not provided
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Jan 20, 2017
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000596538.4
Allele description [Variation Report for NM_000540.3(RYR1):c.7798C>T (p.Arg2600Cys)]
NM_000540.3(RYR1):c.7798C>T (p.Arg2600Cys)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
Assertion and evidence details
Last Updated: May 1, 2024