NM_001127649.3(PEX26):c.571C>T (p.Arg191Trp) AND not provided
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Oct 26, 2016
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000593848.4
Allele description [Variation Report for NM_001127649.3(PEX26):c.571C>T (p.Arg191Trp)]
NM_001127649.3(PEX26):c.571C>T (p.Arg191Trp)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: CN517202
Assertion and evidence details
Last Updated: Apr 9, 2023