NM_020975.6(RET):c.2077C>T (p.Arg693Cys) AND Hirschsprung disease, susceptibility to, 1
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Aug 23, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV003464546.1
Allele description [Variation Report for NM_020975.6(RET):c.2077C>T (p.Arg693Cys)]
NM_020975.6(RET):c.2077C>T (p.Arg693Cys)
Condition(s)
Assertion and evidence details
Last Updated: May 1, 2024