NM_015175.3(NBEAL2):c.1353G>A (p.Pro451=) 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:
- RCV000252387.5
Allele description [Variation Report for NM_015175.3(NBEAL2):c.1353G>A (p.Pro451=)]
NM_015175.3(NBEAL2):c.1353G>A (p.Pro451=)
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
Assertion and evidence details
Last Updated: Mar 10, 2024