NM_001159699.2(FHL1):c.53C>T (p.Ala18Val) AND not provided
- Germline classification:
- Conflicting interpretations of pathogenicity (2 submissions)
- Last evaluated:
- May 4, 2021
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000355754.9
Allele description [Variation Report for NM_001159699.2(FHL1):c.53C>T (p.Ala18Val)]
NM_001159699.2(FHL1):c.53C>T (p.Ala18Val)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
Assertion and evidence details
Last Updated: Feb 20, 2024