NM_000143.4(FH):c.669A>G (p.Lys223=) AND not provided
- Germline classification:
- Likely benign (3 submissions)
- Last evaluated:
- Jan 11, 2024
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000842673.13
Allele description
NM_000143.4(FH):c.669A>G (p.Lys223=)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
Assertion and evidence details
Last Updated: Sep 16, 2024