NM_001365276.2(TNXB):c.1837A>G (p.Ser613Gly) AND Ehlers-Danlos syndrome
- Germline classification:
- Benign (1 submission)
- Last evaluated:
- Jul 10, 2020
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV002276840.3
Allele description [Variation Report for NM_001365276.2(TNXB):c.1837A>G (p.Ser613Gly)]
NM_001365276.2(TNXB):c.1837A>G (p.Ser613Gly)
Condition(s)
Assertion and evidence details
Last Updated: Sep 29, 2024