NM_000277.3(PAH):c.434A>T (p.Asp145Val) AND See cases
- Germline classification:
- Likely pathogenic (1 submission)
- Last evaluated:
- Sep 9, 2020
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV002251980.2
Allele description [Variation Report for NM_000277.3(PAH):c.434A>T (p.Asp145Val)]
NM_000277.3(PAH):c.434A>T (p.Asp145Val)
Condition(s)
- Name:
- See cases [See the Variation display for details]
- Identifiers:
Assertion and evidence details
Last Updated: Jun 17, 2024