NM_001370466.1(NOD2):c.1755G>A (p.Ala585=) AND not provided
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Nov 7, 2018
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000638072.4
Allele description
NM_001370466.1(NOD2):c.1755G>A (p.Ala585=)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: CN517202
Assertion and evidence details
Last Updated: Oct 29, 2022