NM_001035.3(RYR2):c.4209A>G (p.Ala1403=) AND not specified
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- May 22, 2014
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000156583.12
Allele description [Variation Report for NM_001035.3(RYR2):c.4209A>G (p.Ala1403=)]
NM_001035.3(RYR2):c.4209A>G (p.Ala1403=)
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
Assertion and evidence details
Last Updated: Apr 20, 2024