NM_183235.3(RAB27A):c.*1678T>A AND Griscelli syndrome type 2
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Jan 13, 2018
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000336114.5
Allele description [Variation Report for NM_183235.3(RAB27A):c.*1678T>A]
NM_183235.3(RAB27A):c.*1678T>A
Condition(s)
Assertion and evidence details
Last Updated: Dec 24, 2023