Canonical Allele Identifier: PA2825068407
Gene: GAMT HGNC NCBI

Linked Data

ClinVar Variation Id: 1982771
ClinVar RCV Id: RCV002766877
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000147.1:p.Trp102Arg
CA402996214
NM_000156.6:c.304T>C
CA402996215
NM_000156.6:c.304T>A