Canonical Allele Identifier: PA093732
Gene: GAMT HGNC NCBI

Linked Data

ClinVar Variation Id: 328352
ClinVar RCV Id: RCV000389374 RCV001224201
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000147.1:p.Trp45Arg
CA10651554
NM_000156.6:c.133T>A
CA402998098
NM_000156.6:c.133T>C