NM_000701.8(ATP1A1):c.19C>T (p.Arg7Cys) 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:
- RCV002713469.2
Allele description [Variation Report for NM_000701.8(ATP1A1):c.19C>T (p.Arg7Cys)]
NM_000701.8(ATP1A1):c.19C>T (p.Arg7Cys)
Condition(s)
- Name:
- Inborn genetic diseases
- Identifiers:
- MeSH: D030342; MedGen: C0950123
Assertion and evidence details
Last Updated: May 1, 2024