NM_000117.3(EMD):c.672G>A (p.Pro224=) AND not provided
- Germline classification:
- Likely benign (1 submission)
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV004704533.1
Allele description [Variation Report for NM_000117.3(EMD):c.672G>A (p.Pro224=)]
NM_000117.3(EMD):c.672G>A (p.Pro224=)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
Assertion and evidence details
Last Updated: Sep 29, 2024