NM_000705.4(ATP4B):c.77C>T (p.Thr26Met) AND not specified
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Dec 3, 2021
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV004120327.1
Allele description [Variation Report for NM_000705.4(ATP4B):c.77C>T (p.Thr26Met)]
NM_000705.4(ATP4B):c.77C>T (p.Thr26Met)
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
Assertion and evidence details
Last Updated: Jun 2, 2024