NM_000551.4(VHL):c.12G>A (p.Arg4=) AND multiple conditions
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Jan 10, 2024
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000551863.9
Allele description [Variation Report for NM_000551.4(VHL):c.12G>A (p.Arg4=)]
NM_000551.4(VHL):c.12G>A (p.Arg4=)
Condition(s)
Assertion and evidence details
Last Updated: Jul 23, 2024