NM_000016.6(ACADM):c.645T>A (p.Ala215=) AND not provided
- Germline classification:
- Likely benign (2 submissions)
- Last evaluated:
- Nov 1, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV001721308.12
Allele description [Variation Report for NM_000016.6(ACADM):c.645T>A (p.Ala215=)]
NM_000016.6(ACADM):c.645T>A (p.Ala215=)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
Assertion and evidence details
Last Updated: May 1, 2024