NM_001378687.1(ATP2C1):c.-66C>T AND Familial benign pemphigus
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Jan 12, 2018
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000335466.5
Allele description [Variation Report for NM_001378687.1(ATP2C1):c.-66C>T]
NM_001378687.1(ATP2C1):c.-66C>T
Condition(s)
Assertion and evidence details
Last Updated: Feb 4, 2024