NM_000558.5(HBA1):c.396T>C (p.Ser132=) AND HBA1-related disorder
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Jul 22, 2024
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV003979906.2
Allele description [Variation Report for NM_000558.5(HBA1):c.396T>C (p.Ser132=)]
NM_000558.5(HBA1):c.396T>C (p.Ser132=)
Condition(s)
- Name:
- HBA1-related disorder
- Synonyms:
- HBA1-related condition
- Identifiers:
Assertion and evidence details
Last Updated: Oct 13, 2024