NM_002444.3(MSN):c.877C>T (p.Arg293Cys) AND not provided
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Apr 10, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV003661046.1
Allele description [Variation Report for NM_002444.3(MSN):c.877C>T (p.Arg293Cys)]
NM_002444.3(MSN):c.877C>T (p.Arg293Cys)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
Assertion and evidence details
Last Updated: Jun 23, 2024