NM_001958.4(EEF1A2):c.843G>A (p.Ala281=) AND not specified
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Aug 28, 2017
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000422454.2
Allele description
NM_001958.4(EEF1A2):c.843G>A (p.Ala281=)
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
Assertion and evidence details
Last Updated: May 16, 2021