Allele Registry

Canonical Allele Identifier: PA891845843

Gene: GAMT HGNC NCBI

ClinVar Variation Id: 566179

HGVS (amino-acid)	Matching Registered Transcripts
NP_000147.1:p.Met50Ile	CA402998057 NM_000156.6:c.150G>T CA402998058 NM_000156.6:c.150G>A CA402998059 NM_000156.6:c.150G>C