NM_000540.3(RYR1):c.4758G>A (p.Pro1586=) AND not specified
- Germline classification:
- Likely benign (1 submission)
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000253584.9
Allele description
NM_000540.3(RYR1):c.4758G>A (p.Pro1586=)
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
Assertion and evidence details
Last Updated: Mar 10, 2024