NM_052906.5(ELFN2):c.1279G>C (p.Glu427Gln) AND not specified
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Jul 11, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV004353860.1
Allele description [Variation Report for NM_052906.5(ELFN2):c.1279G>C (p.Glu427Gln)]
NM_052906.5(ELFN2):c.1279G>C (p.Glu427Gln)
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
Assertion and evidence details
Last Updated: Sep 8, 2024