NM_022089.4(ATP13A2):c.453C>T (p.Ser151=) AND not provided
- Germline classification:
- Benign/Likely benign (3 submissions)
- Last evaluated:
- Mar 19, 2021
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000710714.15
Allele description [Variation Report for NM_022089.4(ATP13A2):c.453C>T (p.Ser151=)]
NM_022089.4(ATP13A2):c.453C>T (p.Ser151=)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
Assertion and evidence details
Last Updated: Sep 8, 2024