NM_000558.5(HBA1):c.396T>C (p.Ser132=) AND alpha Thalassemia
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Aug 9, 2017
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV001834633.1
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)
Assertion and evidence details
Last Updated: Oct 13, 2024