NM_003722.5(TP63):c.1788G>A (p.Ala596=) AND TP63-Related Spectrum Disorders
- Germline classification:
- Benign (1 submission)
- Last evaluated:
- Jan 8, 2024
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV002064892.13
Allele description [Variation Report for NM_003722.5(TP63):c.1788G>A (p.Ala596=)]
NM_003722.5(TP63):c.1788G>A (p.Ala596=)
Condition(s)
- Name:
- TP63-Related Spectrum Disorders
- Identifiers:
- MedGen: CN239305
Assertion and evidence details
Last Updated: May 19, 2024