NM_004385.5(VCAN):c.7420G>A (p.Ala2474Thr) AND Inborn genetic diseases
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- May 3, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV003284353.2
Allele description [Variation Report for NM_004385.5(VCAN):c.7420G>A (p.Ala2474Thr)]
NM_004385.5(VCAN):c.7420G>A (p.Ala2474Thr)
Condition(s)
- Name:
- Inborn genetic diseases
- Identifiers:
- MeSH: D030342; MedGen: C0950123
Assertion and evidence details
Last Updated: May 1, 2024