NM_000018.4(ACADVL):c.787G>A (p.Ala263Thr) AND not provided
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Jun 28, 2013
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000077924.4
Allele description
NM_000018.4(ACADVL):c.787G>A (p.Ala263Thr)
Condition(s)
- Identifiers:
- MedGen: CN517202
Assertion and evidence details
Last Updated: Dec 4, 2021