NM_000540.3(RYR1):c.7121C>T (p.Ser2374Leu) AND not provided
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Jul 2, 2018
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000493566.2
Allele description [Variation Report for NM_000540.3(RYR1):c.7121C>T (p.Ser2374Leu)]
NM_000540.3(RYR1):c.7121C>T (p.Ser2374Leu)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: CN517202
Assertion and evidence details
Last Updated: Nov 5, 2022