NM_001001331.4(ATP2B2):c.1891G>A (p.Val631Met) AND not provided
- Germline classification:
- Benign (2 submissions)
- Last evaluated:
- Jan 1, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000954243.7
Allele description
NM_001001331.4(ATP2B2):c.1891G>A (p.Val631Met)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: CN517202
Assertion and evidence details
Last Updated: Apr 23, 2023