NM_002016.2(FLG):c.4029G>A (p.Val1343=) AND not provided
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Sep 1, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV003408984.9
Allele description [Variation Report for NM_002016.2(FLG):c.4029G>A (p.Val1343=)]
NM_002016.2(FLG):c.4029G>A (p.Val1343=)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
Assertion and evidence details
Last Updated: Oct 8, 2024