Canonical Allele Identifier: PA093700
Gene: GAMT HGNC NCBI

Linked Data

ClinVar Variation Id: 2570638
ClinVar RCV Id: RCV003307397
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000147.1:p.Leu197Pro
CA402990982
NM_000156.6:c.590T>C