NM_000143.3(FH):c.695G>A (p.Gly232Glu) AND not provided
- Germline classification:
- Uncertain significance (2 submissions)
- Last evaluated:
- Mar 17, 2022
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000153238.16
Allele description [Variation Report for NM_000143.3(FH):c.695G>A (p.Gly232Glu)]
NM_000143.3(FH):c.695G>A (p.Gly232Glu)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
Assertion and evidence details
Last Updated: Sep 29, 2024