NM_001082486.2(ACD):c.894T>A (p.Pro298=) AND Inborn genetic diseases
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- May 26, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV003307689.2
Allele description [Variation Report for NM_001082486.2(ACD):c.894T>A (p.Pro298=)]
NM_001082486.2(ACD):c.894T>A (p.Pro298=)
Condition(s)
- Name:
- Inborn genetic diseases
- Identifiers:
- MeSH: D030342; MedGen: C0950123
Assertion and evidence details
Last Updated: Nov 3, 2024