NM_000238.4(KCNH2):c.1809C>T (p.Gly603=) AND not provided
- Germline classification:
- Benign (3 submissions)
- Last evaluated:
- Oct 11, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000712074.19
Allele description [Variation Report for NM_000238.4(KCNH2):c.1809C>T (p.Gly603=)]
NM_000238.4(KCNH2):c.1809C>T (p.Gly603=)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
Assertion and evidence details
Last Updated: Sep 1, 2024