NM_005477.3(HCN4):c.3396C>T (p.Ser1132=) AND Cardiovascular phenotype
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Apr 4, 2016
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000620308.3
Allele description [Variation Report for NM_005477.3(HCN4):c.3396C>T (p.Ser1132=)]
NM_005477.3(HCN4):c.3396C>T (p.Ser1132=)
Condition(s)
- Name:
- Cardiovascular phenotype
- Identifiers:
- MedGen: CN230736
Assertion and evidence details
Last Updated: May 1, 2024