NM_001943.5(DSG2):c.2690C>A (p.Ala897Asp) AND not provided
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Jan 16, 2013
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000181232.2
Allele description [Variation Report for NM_001943.5(DSG2):c.2690C>A (p.Ala897Asp)]
NM_001943.5(DSG2):c.2690C>A (p.Ala897Asp)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
Assertion and evidence details
Last Updated: Feb 20, 2024