NM_002461.3(MVD):c.676C>T (p.Arg226Trp) AND not specified
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- May 24, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV004295651.1
Allele description [Variation Report for NM_002461.3(MVD):c.676C>T (p.Arg226Trp)]
NM_002461.3(MVD):c.676C>T (p.Arg226Trp)
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
Assertion and evidence details
Last Updated: Nov 24, 2024