NM_015466.4(PTPN23):c.1291C>T (p.Arg431Trp) AND not provided
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Sep 1, 2022
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV001869201.2
Allele description [Variation Report for NM_015466.4(PTPN23):c.1291C>T (p.Arg431Trp)]
NM_015466.4(PTPN23):c.1291C>T (p.Arg431Trp)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
Assertion and evidence details
Last Updated: Mar 16, 2024