NM_000143.4(FH):c.1385A>G (p.His462Arg) AND not provided
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Jul 8, 2021
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV002592580.10
Allele description [Variation Report for NM_000143.4(FH):c.1385A>G (p.His462Arg)]
NM_000143.4(FH):c.1385A>G (p.His462Arg)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
Assertion and evidence details
Last Updated: Oct 20, 2024