NM_000238.4(KCNH2):c.2684C>T (p.Thr895Met) AND SUDDEN INFANT DEATH 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:
- RCV000058151.11
Allele description [Variation Report for NM_000238.4(KCNH2):c.2684C>T (p.Thr895Met)]
NM_000238.4(KCNH2):c.2684C>T (p.Thr895Met)
Condition(s)
Assertion and evidence details
Last Updated: Aug 25, 2024