NM_016203.4(PRKAG2):c.665A>T (p.His222Leu) AND Lethal congenital glycogen storage disease of heart
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Mar 19, 2022
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV002917759.3
Allele description [Variation Report for NM_016203.4(PRKAG2):c.665A>T (p.His222Leu)]
NM_016203.4(PRKAG2):c.665A>T (p.His222Leu)
Condition(s)
Assertion and evidence details
Last Updated: Sep 29, 2024