NM_017882.3(CLN6):c.728C>T (p.Ala243Val) AND multiple conditions
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- May 3, 2022
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV002478655.8
Allele description [Variation Report for NM_017882.3(CLN6):c.728C>T (p.Ala243Val)]
NM_017882.3(CLN6):c.728C>T (p.Ala243Val)
Condition(s)
Assertion and evidence details
Last Updated: Aug 18, 2024