NM_000238.4(KCNH2):c.1039C>T (p.Pro347Ser) AND KCNH2-related disorder
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Aug 17, 2022
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV004549481.1
Allele description [Variation Report for NM_000238.4(KCNH2):c.1039C>T (p.Pro347Ser)]
NM_000238.4(KCNH2):c.1039C>T (p.Pro347Ser)
Condition(s)
- Name:
- KCNH2-related disorder
- Synonyms:
- KCNH2-related disorders; KCNH2-related condition
- Identifiers:
Assertion and evidence details
Last Updated: Aug 25, 2024