NM_001082.5(CYP4F2):c.1297G>A (p.Val433Met) AND CYP4F2-related disorder
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Jul 22, 2021
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV003977584.1
Allele description [Variation Report for NM_001082.5(CYP4F2):c.1297G>A (p.Val433Met)]
NM_001082.5(CYP4F2):c.1297G>A (p.Val433Met)
Condition(s)
- Name:
- CYP4F2-related disorder
- Synonyms:
- CYP4F2-related condition
- Identifiers:
Assertion and evidence details
Last Updated: Jun 9, 2024