NM_000517.6(HBA2):c.358C>G (p.Pro120Ala) AND not provided
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Aug 31, 2021
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV001284149.2
Allele description [Variation Report for NM_000517.6(HBA2):c.358C>G (p.Pro120Ala)]
NM_000517.6(HBA2):c.358C>G (p.Pro120Ala)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: CN517202
Assertion and evidence details
Last Updated: May 27, 2023