NM_181789.4(GLDN):c.593A>G (p.His198Arg) AND Inborn genetic diseases
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Dec 17, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV004393028.1
Allele description [Variation Report for NM_181789.4(GLDN):c.593A>G (p.His198Arg)]
NM_181789.4(GLDN):c.593A>G (p.His198Arg)
Condition(s)
- Name:
- Inborn genetic diseases
- Identifiers:
- MeSH: D030342; MedGen: C0950123
-
LINC02523 long intergenic non-protein coding RNA 2523 [Homo sapiens]
LINC02523 long intergenic non-protein coding RNA 2523 [Homo sapiens]Gene ID:643623Gene
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Last Updated: May 7, 2024