NM_000891.3(KCNJ2):c.566G>T (p.Arg189Ile) AND Congenital long QT syndrome
- 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:
- RCV000058320.3
Allele description [Variation Report for NM_000891.3(KCNJ2):c.566G>T (p.Arg189Ile)]
NM_000891.3(KCNJ2):c.566G>T (p.Arg189Ile)
Condition(s)
Assertion and evidence details
Last Updated: Mar 4, 2023