NM_030665.4(RAI1):c.585C>T (p.Asn195=) AND Inborn genetic diseases
- Germline classification:
- Benign (1 submission)
- Last evaluated:
- May 31, 2019
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV002359202.2
Allele description [Variation Report for NM_030665.4(RAI1):c.585C>T (p.Asn195=)]
NM_030665.4(RAI1):c.585C>T (p.Asn195=)
Condition(s)
- Name:
- Inborn genetic diseases
- Identifiers:
- MeSH: D030342; MedGen: C0950123
-
Coprosma rhynchocarpa (1)
Taxonomy
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Last Updated: Oct 8, 2024