NM_000540.3(RYR1):c.11980G>A (p.Val3994Met) AND Inborn genetic diseases
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Dec 19, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV004447170.1
Allele description [Variation Report for NM_000540.3(RYR1):c.11980G>A (p.Val3994Met)]
NM_000540.3(RYR1):c.11980G>A (p.Val3994Met)
Condition(s)
- Name:
- Inborn genetic diseases
- Identifiers:
- MeSH: D030342; MedGen: C0950123
-
Crisp2 cysteine-rich secretory protein 2 [Rattus norvegicus]
Crisp2 cysteine-rich secretory protein 2 [Rattus norvegicus]Gene ID:360445Gene
Your browsing activity is empty.
Activity recording is turned off.
See more...Assertion and evidence details
Last Updated: May 7, 2024