NM_002016.2(FLG):c.3436C>A (p.His1146Asn) AND not provided
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Jun 1, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV003408991.8
Allele description [Variation Report for NM_002016.2(FLG):c.3436C>A (p.His1146Asn)]
NM_002016.2(FLG):c.3436C>A (p.His1146Asn)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
Assertion and evidence details
Last Updated: Aug 4, 2024