NM_000238.4(KCNH2):c.2607G>A (p.Pro869=) AND not specified
- Germline classification:
- Benign (1 submission)
- Last evaluated:
- Oct 1, 2014
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000181736.9
Allele description [Variation Report for NM_000238.4(KCNH2):c.2607G>A (p.Pro869=)]
NM_000238.4(KCNH2):c.2607G>A (p.Pro869=)
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
Assertion and evidence details
Last Updated: Oct 13, 2024