NM_152419.3(HGSNAT):c.1750G>A (p.Val584Ile) AND Inborn genetic diseases
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- May 24, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV003284503.2
Allele description [Variation Report for NM_152419.3(HGSNAT):c.1750G>A (p.Val584Ile)]
NM_152419.3(HGSNAT):c.1750G>A (p.Val584Ile)
Condition(s)
- Name:
- Inborn genetic diseases
- Identifiers:
- MeSH: D030342; MedGen: C0950123
-
D13Mc1 DNA segment, Chr 13, McClelland 1 [Mus musculus]
D13Mc1 DNA segment, Chr 13, McClelland 1 [Mus musculus]Gene ID:53709Gene
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Last Updated: May 1, 2024