NM_022489.4(INF2):c.1275A>C (p.Pro425=) AND not provided
- Germline classification:
- Benign (1 submission)
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV004715387.1
Allele description [Variation Report for NM_022489.4(INF2):c.1275A>C (p.Pro425=)]
NM_022489.4(INF2):c.1275A>C (p.Pro425=)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
Assertion and evidence details
Last Updated: Sep 29, 2024