NM_001375978.1(CHRM3):c.328C>T (p.Leu110=) AND not provided
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Jan 24, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000894535.5
Allele description
NM_001375978.1(CHRM3):c.328C>T (p.Leu110=)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
Assertion and evidence details
Last Updated: Feb 20, 2024