NM_000143.4(FH):c.655G>A (p.Asp219Asn) AND not provided
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Jan 25, 2024
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV002523294.3
Allele description [Variation Report for NM_000143.4(FH):c.655G>A (p.Asp219Asn)]
NM_000143.4(FH):c.655G>A (p.Asp219Asn)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
Assertion and evidence details
Last Updated: Jul 15, 2024