NM_001035.3(RYR2):c.14733G>A (p.Gln4911=) AND not provided
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Oct 28, 2015
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000205512.5
Allele description
NM_001035.3(RYR2):c.14733G>A (p.Gln4911=)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: CN517202
Assertion and evidence details
Last Updated: Dec 24, 2022