NM_002016.2(FLG):c.2938C>G (p.His980Asp) AND not specified
- Germline classification:
- Benign (2 submissions)
- Last evaluated:
- Mar 28, 2016
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000456001.6
Allele description [Variation Report for NM_002016.2(FLG):c.2938C>G (p.His980Asp)]
NM_002016.2(FLG):c.2938C>G (p.His980Asp)
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
Assertion and evidence details
Last Updated: Dec 24, 2023