NM_003924.4(PHOX2B):c.450C>G (p.Arg150=) AND Haddad syndrome
- Germline classification:
- Benign (1 submission)
- Last evaluated:
- Jan 19, 2024
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV001507133.8
Allele description [Variation Report for NM_003924.4(PHOX2B):c.450C>G (p.Arg150=)]
NM_003924.4(PHOX2B):c.450C>G (p.Arg150=)
Condition(s)
Assertion and evidence details
Last Updated: May 1, 2024