NM_001040142.2(SCN2A):c.56G>A (p.Arg19Lys) AND Inborn genetic diseases
- Germline classification:
- Benign (1 submission)
- Last evaluated:
- Jan 8, 2016
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV002312496.9
Allele description [Variation Report for NM_001040142.2(SCN2A):c.56G>A (p.Arg19Lys)]
NM_001040142.2(SCN2A):c.56G>A (p.Arg19Lys)
Condition(s)
- Name:
- Inborn genetic diseases
- Identifiers:
- MeSH: D030342; MedGen: C0950123
-
alpha-expansin 6, partial [Gossypium arboreum]
alpha-expansin 6, partial [Gossypium arboreum]gi|150022340|gb|ABR57496.1|Protein
-
LEGCYC2, partial [Bauhinia kalantha]
LEGCYC2, partial [Bauhinia kalantha]gi|992216220|gb|AMH83194.1|Protein
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See more...Assertion and evidence details
Last Updated: Nov 10, 2024