NM_000038.6(APC):c.7577A>G (p.His2526Arg) AND not provided
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Dec 16, 2022
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000236866.2
Allele description [Variation Report for NM_000038.6(APC):c.7577A>G (p.His2526Arg)]
NM_000038.6(APC):c.7577A>G (p.His2526Arg)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
Assertion and evidence details
Last Updated: Oct 20, 2024