NM_001363118.2(SLC52A2):c.550C>T (p.Pro184Ser) AND Brown-Vialetto-van Laere syndrome 2
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Nov 1, 2022
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV003077532.2
Allele description [Variation Report for NM_001363118.2(SLC52A2):c.550C>T (p.Pro184Ser)]
NM_001363118.2(SLC52A2):c.550C>T (p.Pro184Ser)
Condition(s)
Assertion and evidence details
Last Updated: May 1, 2024