NM_001173523.2(PCDH7):c.1704C>T (p.Ala568=) AND not provided
- Germline classification:
- Benign (2 submissions)
- Last evaluated:
- Dec 31, 2019
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000970834.5
Allele description [Variation Report for NM_001173523.2(PCDH7):c.1704C>T (p.Ala568=)]
NM_001173523.2(PCDH7):c.1704C>T (p.Ala568=)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
Assertion and evidence details
Last Updated: Sep 29, 2024