NM_016203.4(PRKAG2):c.247C>T (p.Pro83Ser) AND not provided
- Germline classification:
- Likely benign (5 submissions)
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV001529077.8
Allele description [Variation Report for NM_016203.4(PRKAG2):c.247C>T (p.Pro83Ser)]
NM_016203.4(PRKAG2):c.247C>T (p.Pro83Ser)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
Assertion and evidence details
Last Updated: May 1, 2024