NM_001378969.1(KCND3):c.1372-6dup AND not specified
- Germline classification:
- Benign (1 submission)
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV001701280.2
Allele description [Variation Report for NM_001378969.1(KCND3):c.1372-6dup]
NM_001378969.1(KCND3):c.1372-6dup
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
Assertion and evidence details
Last Updated: Sep 29, 2024