NM_000117.3(EMD):c.396C>T (p.His132=) AND Cardiovascular phenotype
- Germline classification:
- Benign (1 submission)
- Last evaluated:
- Mar 7, 2017
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000621249.4
Allele description [Variation Report for NM_000117.3(EMD):c.396C>T (p.His132=)]
NM_000117.3(EMD):c.396C>T (p.His132=)
Condition(s)
- Name:
- Cardiovascular phenotype
- Identifiers:
- MedGen: CN230736
Assertion and evidence details
Last Updated: May 12, 2024