NM_144670.6(A2ML1):c.2197T>C (p.Phe733Leu) AND A2ML1-related disorder
- Germline classification:
- Benign (1 submission)
- Last evaluated:
- Oct 16, 2019
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV003942382.1
Allele description
NM_144670.6(A2ML1):c.2197T>C (p.Phe733Leu)
Condition(s)
- Name:
- A2ML1-related disorder
- Synonyms:
- A2ML1-related condition
- Identifiers:
Assertion and evidence details
Last Updated: Sep 29, 2024