NM_000540.3(RYR1):c.1516G>A (p.Ala506Thr) AND Inborn genetic diseases
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Jan 25, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV003167835.2
Allele description [Variation Report for NM_000540.3(RYR1):c.1516G>A (p.Ala506Thr)]
NM_000540.3(RYR1):c.1516G>A (p.Ala506Thr)
Condition(s)
- Name:
- Inborn genetic diseases
- Identifiers:
- MeSH: D030342; MedGen: C0950123
-
5033417F24Rik RIKEN cDNA 5033417F24 gene [Mus musculus]
5033417F24Rik RIKEN cDNA 5033417F24 gene [Mus musculus]Gene ID:75995Gene
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Last Updated: Oct 13, 2024