NM_144997.7(FLCN):c.586A>G (p.Ile196Val) AND not provided
- Germline classification:
- Uncertain significance (2 submissions)
- Last evaluated:
- Dec 14, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000034793.5
Allele description [Variation Report for NM_144997.7(FLCN):c.586A>G (p.Ile196Val)]
NM_144997.7(FLCN):c.586A>G (p.Ile196Val)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
Assertion and evidence details
Last Updated: Sep 29, 2024