NM_000551.4(VHL):c.627A>T (p.Gln209His) AND multiple conditions
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Feb 26, 2020
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV001361052.8
Allele description [Variation Report for NM_000551.4(VHL):c.627A>T (p.Gln209His)]
NM_000551.4(VHL):c.627A>T (p.Gln209His)
Condition(s)
Assertion and evidence details
Last Updated: Mar 5, 2024