NM_000277.3(PAH):c.66A>C (p.Thr22=) AND Phenylketonuria
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Oct 6, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV002180060.5
Allele description [Variation Report for NM_000277.3(PAH):c.66A>C (p.Thr22=)]
NM_000277.3(PAH):c.66A>C (p.Thr22=)
Condition(s)
Assertion and evidence details
Last Updated: Feb 28, 2024