NM_003924.4(PHOX2B):c.642C>T (p.Gly214=) AND Haddad syndrome
- Germline classification:
- Benign (1 submission)
- Last evaluated:
- Jan 22, 2024
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000475781.11
Allele description [Variation Report for NM_003924.4(PHOX2B):c.642C>T (p.Gly214=)]
NM_003924.4(PHOX2B):c.642C>T (p.Gly214=)
Condition(s)
Assertion and evidence details
Last Updated: Aug 4, 2024