NM_145239.3(PRRT2):c.696C>G (p.His232Gln) AND not provided
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Mar 1, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV003427525.9
Allele description [Variation Report for NM_145239.3(PRRT2):c.696C>G (p.His232Gln)]
NM_145239.3(PRRT2):c.696C>G (p.His232Gln)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
Assertion and evidence details
Last Updated: Oct 8, 2024