NM_002633.3(PGM1):c.*231C>T AND Congenital disorder of glycosylation
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Jun 14, 2016
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000348511.5
Allele description [Variation Report for NM_002633.3(PGM1):c.*231C>T]
NM_002633.3(PGM1):c.*231C>T
Condition(s)
Assertion and evidence details
Last Updated: Apr 9, 2023