NM_145728.3(SYNM):c.576C>T (p.Ala192=) AND SYNM-related disorder
- Germline classification:
- Benign (1 submission)
- Last evaluated:
- Jun 3, 2021
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV003921607.1
Allele description [Variation Report for NM_145728.3(SYNM):c.576C>T (p.Ala192=)]
NM_145728.3(SYNM):c.576C>T (p.Ala192=)
Condition(s)
- Name:
- SYNM-related disorder
- Synonyms:
- SYNM-related condition
- Identifiers:
Assertion and evidence details
Last Updated: May 19, 2024