NM_000517.6(HBA2):c.414C>T (p.Thr138=) AND HBA2-related disorder
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Jun 22, 2020
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV003950541.1
Allele description
NM_000517.6(HBA2):c.414C>T (p.Thr138=)
Condition(s)
- Name:
- HBA2-related disorder
- Synonyms:
- HBA2-related condition
- Identifiers:
Assertion and evidence details
Last Updated: Sep 29, 2024