NM_000518.5(HBB):c.154C>A (p.Pro52Thr) AND not provided
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Dec 5, 2019
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV001284629.1
Allele description [Variation Report for NM_000518.5(HBB):c.154C>A (p.Pro52Thr)]
NM_000518.5(HBB):c.154C>A (p.Pro52Thr)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: CN517202
Assertion and evidence details
Last Updated: Apr 23, 2022