Canonical Allele Identifier: PA288885
Gene: GAMT HGNC NCBI

Linked Data

ClinVar Variation Id: 21068
ClinVar RCV Id: RCV000020144 RCV000117117 RCV000272863 RCV000311501 RCV000676877 RCV001520666 RCV002311515
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000147.1:p.Thr209Met
CA288884
NM_000156.6:c.626C>T