NM_020975.6(RET):c.785T>C (p.Val262Ala) AND RET-related disorder
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Jan 31, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV004528165.1
Allele description [Variation Report for NM_020975.6(RET):c.785T>C (p.Val262Ala)]
NM_020975.6(RET):c.785T>C (p.Val262Ala)
Condition(s)
- Name:
- RET-related disorder
- Synonyms:
- RET-related disorders; RET-related condition; RET-related disease
- Identifiers:
Assertion and evidence details
Last Updated: Jun 9, 2024