NM_014251.3(SLC25A13):c.1710G>T (p.Leu570=) AND not provided
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Sep 27, 2017
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000729323.4
Allele description [Variation Report for NM_014251.3(SLC25A13):c.1710G>T (p.Leu570=)]
NM_014251.3(SLC25A13):c.1710G>T (p.Leu570=)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: CN517202
-
Homo sapiens peripheral myelin protein 2 (PMP2), transcript variant 1, mRNA
Homo sapiens peripheral myelin protein 2 (PMP2), transcript variant 1, mRNAgi|1143077036|ref|NM_002677.4|Nucleotide
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Last Updated: Apr 1, 2023