NM_000152.5(GAA):c.1278C>T (p.Ala426=) AND Cardiovascular phenotype
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Apr 16, 2020
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV002443486.2
Allele description [Variation Report for NM_000152.5(GAA):c.1278C>T (p.Ala426=)]
NM_000152.5(GAA):c.1278C>T (p.Ala426=)
Condition(s)
- Name:
- Cardiovascular phenotype
- Identifiers:
- MedGen: CN230736
Assertion and evidence details
Last Updated: Sep 29, 2024