NM_000277.3(PAH):c.678G>C (p.Gln226His) AND not provided
- Germline classification:
- not provided (1 submission)
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000089034.1
Allele description [Variation Report for NM_000277.3(PAH):c.678G>C (p.Gln226His)]
NM_000277.3(PAH):c.678G>C (p.Gln226His)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
Assertion and evidence details
Last Updated: Feb 14, 2024