NM_000551.4(VHL):c.339A>C (p.Arg113=) AND multiple conditions
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Aug 31, 2022
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV002597019.2
Allele description [Variation Report for NM_000551.4(VHL):c.339A>C (p.Arg113=)]
NM_000551.4(VHL):c.339A>C (p.Arg113=)
Condition(s)
Assertion and evidence details
Last Updated: Feb 28, 2024