NM_000277.3(PAH):c.1098C>G (p.Pro366=) AND Phenylketonuria
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Dec 4, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV003597710.1
Allele description [Variation Report for NM_000277.3(PAH):c.1098C>G (p.Pro366=)]
NM_000277.3(PAH):c.1098C>G (p.Pro366=)
Condition(s)
Assertion and evidence details
Last Updated: Feb 28, 2024