NM_000551.4(VHL):c.82G>A (p.Asp28Asn) AND multiple conditions
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Sep 21, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000818951.7
Allele description [Variation Report for NM_000551.4(VHL):c.82G>A (p.Asp28Asn)]
NM_000551.4(VHL):c.82G>A (p.Asp28Asn)
Condition(s)
Assertion and evidence details
Last Updated: Jul 23, 2024