NM_001114134.2(EPB42):c.654+7G>A AND not specified
- Germline classification:
- Benign (1 submission)
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000242857.5
Allele description [Variation Report for NM_001114134.2(EPB42):c.654+7G>A]
NM_001114134.2(EPB42):c.654+7G>A
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
Assertion and evidence details
Last Updated: Mar 10, 2024