NM_003640.5(ELP1):c.2199G>A (p.Leu733=) AND not provided
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Sep 29, 2022
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV002612400.2
Allele description [Variation Report for NM_003640.5(ELP1):c.2199G>A (p.Leu733=)]
NM_003640.5(ELP1):c.2199G>A (p.Leu733=)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
Assertion and evidence details
Last Updated: Feb 14, 2024