NM_001999.4(FBN2):c.976C>T (p.Pro326Ser) AND Cardiovascular phenotype
- Germline classification:
- Benign (1 submission)
- Last evaluated:
- Nov 13, 2014
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000254151.2
Allele description
NM_001999.4(FBN2):c.976C>T (p.Pro326Ser)
Condition(s)
- Name:
- Cardiovascular phenotype
- Identifiers:
- MedGen: CN230736
Assertion and evidence details
Last Updated: Nov 19, 2022