NM_001482.3(GATM):c.1252T>C (p.Leu418=) AND not provided
- Germline classification:
- Benign (4 submissions)
- Last evaluated:
- Jul 29, 2020
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000711746.19
Allele description [Variation Report for NM_001482.3(GATM):c.1252T>C (p.Leu418=)]
NM_001482.3(GATM):c.1252T>C (p.Leu418=)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
Assertion and evidence details
Last Updated: Oct 13, 2024