Canonical Allele Identifier: PA2742005630
Gene: GAMT HGNC NCBI

Linked Data

ClinVar Variation Id: 2683727
ClinVar RCV Id: RCV003482173
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_620279.1:p.Lys39Glu
CA402998134
NM_138924.3:c.115A>G