NM_000517.6(HBA2):c.38C>A (p.Ala13Asp) AND not provided
- Germline classification:
- Conflicting interpretations of pathogenicity (2 submissions)
- Last evaluated:
- Nov 24, 2021
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV001284151.16
Allele description [Variation Report for NM_000517.6(HBA2):c.38C>A (p.Ala13Asp)]
NM_000517.6(HBA2):c.38C>A (p.Ala13Asp)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
Assertion and evidence details
Last Updated: Oct 20, 2024