NM_022089.4(ATP13A2):c.132A>G (p.Pro44=) AND History of neurodevelopmental disorder
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Jun 9, 2016
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000716001.1
Allele description
NM_022089.4(ATP13A2):c.132A>G (p.Pro44=)
Condition(s)
- Name:
- History of neurodevelopmental disorder
- Identifiers:
- MedGen: C2711754
Assertion and evidence details
Last Updated: Nov 19, 2022