NM_002016.2(FLG):c.7252G>A (p.Val2418Met) AND not provided
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Jul 9, 2018
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV001562294.2
Allele description [Variation Report for NM_002016.2(FLG):c.7252G>A (p.Val2418Met)]
NM_002016.2(FLG):c.7252G>A (p.Val2418Met)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
Assertion and evidence details
Last Updated: Dec 24, 2023