NM_000238.4(KCNH2):c.1942G>A (p.Gly648Ser) 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:
- RCV000058064.5
Allele description [Variation Report for NM_000238.4(KCNH2):c.1942G>A (p.Gly648Ser)]
NM_000238.4(KCNH2):c.1942G>A (p.Gly648Ser)
Condition(s)
Assertion and evidence details
Last Updated: Nov 5, 2022