Canonical Allele Identifier: PA2825068496
Gene: GAMT HGNC NCBI

Linked Data

ClinVar Variation Id: 2060933
ClinVar RCV Id: RCV002948105 RCV003367914
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000147.1:p.Ala156Thr
CA9043638
NM_000156.6:c.466G>A