NM_001374353.1(GLI2):c.4636A>G (p.Met1546Val) AND Inborn genetic diseases
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Feb 17, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV003210689.2
Allele description [Variation Report for NM_001374353.1(GLI2):c.4636A>G (p.Met1546Val)]
NM_001374353.1(GLI2):c.4636A>G (p.Met1546Val)
Condition(s)
- Name:
- Inborn genetic diseases
- Identifiers:
- MeSH: D030342; MedGen: C0950123
-
Pisa armata voucher IEOCD-GB08-180 large subunit ribosomal RNA gene, partial seq...
Pisa armata voucher IEOCD-GB08-180 large subunit ribosomal RNA gene, partial sequence; mitochondrialgi|2647705730|gb|PP118336.1|Nucleotide
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Last Updated: May 1, 2024