NM_170606.3(KMT2C):c.8502A>T (p.Glu2834Asp) AND atypical cerebral palsy
- Germline classification:
- Uncertain significance (1 submission)
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000655963.2
Allele description [Variation Report for NM_170606.3(KMT2C):c.8502A>T (p.Glu2834Asp)]
NM_170606.3(KMT2C):c.8502A>T (p.Glu2834Asp)
Condition(s)
- Name:
- atypical cerebral palsy
- Identifiers:
- MedGen: CN479605
Assertion and evidence details
Last Updated: Oct 8, 2024