NM_000540.3(RYR1):c.7536C>T (p.Ile2512=) AND not provided
- Germline classification:
- Likely benign (2 submissions)
- Last evaluated:
- May 1, 2024
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000655719.29
Allele description [Variation Report for NM_000540.3(RYR1):c.7536C>T (p.Ile2512=)]
NM_000540.3(RYR1):c.7536C>T (p.Ile2512=)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
Assertion and evidence details
Last Updated: Oct 13, 2024