NM_001128840.3(CACNA1D):c.5358T>C (p.His1786=) AND not provided
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Mar 20, 2022
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV002741474.3
Allele description [Variation Report for NM_001128840.3(CACNA1D):c.5358T>C (p.His1786=)]
NM_001128840.3(CACNA1D):c.5358T>C (p.His1786=)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
Assertion and evidence details
Last Updated: Sep 29, 2024