NM_000551.4(VHL):c.183C>A (p.Pro61=) AND multiple conditions
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Jun 25, 2022
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV001456043.14
Allele description [Variation Report for NM_000551.4(VHL):c.183C>A (p.Pro61=)]
NM_000551.4(VHL):c.183C>A (p.Pro61=)
Condition(s)
Assertion and evidence details
Last Updated: Sep 29, 2024