NM_000203.5(IDUA):c.1303C>T (p.Arg435Cys) AND Inborn genetic diseases
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Jul 9, 2021
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV002786003.2
Allele description [Variation Report for NM_000203.5(IDUA):c.1303C>T (p.Arg435Cys)]
NM_000203.5(IDUA):c.1303C>T (p.Arg435Cys)
Condition(s)
- Name:
- Inborn genetic diseases
- Identifiers:
- MeSH: D030342; MedGen: C0950123
Assertion and evidence details
Last Updated: Oct 13, 2024