NM_000138.5(FBN1):c.7661G>A (p.Arg2554Gln) AND not provided
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Apr 11, 2024
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000766961.6
Allele description [Variation Report for NM_000138.5(FBN1):c.7661G>A (p.Arg2554Gln)]
NM_000138.5(FBN1):c.7661G>A (p.Arg2554Gln)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
Assertion and evidence details
Last Updated: Sep 29, 2024