Canonical Allele Identifier: PA093632
Gene: GAMT HGNC NCBI

Linked Data

ClinVar Variation Id: 8304
ClinVar RCV Id: RCV000008802 RCV001762039
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000147.1:p.Cys169Tyr
CA254379
NM_000156.6:c.506G>A