NM_000264.5(PTCH1):c.801G>A (p.Glu267=) AND PTCH1-related condition
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Sep 20, 2022
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV003945108.1
Allele description [Variation Report for NM_000264.5(PTCH1):c.801G>A (p.Glu267=)]
NM_000264.5(PTCH1):c.801G>A (p.Glu267=)
Condition(s)
- Name:
- PTCH1-related condition
- Identifiers:
Assertion and evidence details
Last Updated: Apr 20, 2024