NM_003055.3(SLC18A3):c.916G>T (p.Ala306Ser) AND Inborn genetic diseases
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Apr 19, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV003289758.9
Allele description [Variation Report for NM_003055.3(SLC18A3):c.916G>T (p.Ala306Ser)]
NM_003055.3(SLC18A3):c.916G>T (p.Ala306Ser)
Condition(s)
- Name:
- Inborn genetic diseases
- Identifiers:
- MeSH: D030342; MedGen: C0950123
Assertion and evidence details
Last Updated: Jun 2, 2024