Canonical Allele Identifier: PA093690
Gene: GAMT HGNC NCBI

Linked Data

ClinVar Variation Id: 1312506
ClinVar RCV Id: RCV001761400 RCV003298978
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000147.1:p.Leu166Pro
CA402994573
NM_000156.6:c.497T>C