NM_001384140.1(PCDH15):c.1912C>T (p.Leu638=) AND not provided
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Dec 20, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000941544.8
Allele description [Variation Report for NM_001384140.1(PCDH15):c.1912C>T (p.Leu638=)]
NM_001384140.1(PCDH15):c.1912C>T (p.Leu638=)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
Assertion and evidence details
Last Updated: Feb 20, 2024