NM_003924.4(PHOX2B):c.234C>T (p.Tyr78=) AND not provided
- Germline classification:
- Benign (1 submission)
- Last evaluated:
- May 17, 2016
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000590552.3
Allele description
NM_003924.4(PHOX2B):c.234C>T (p.Tyr78=)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
Assertion and evidence details
Last Updated: May 1, 2024