Canonical Allele Identifier: PA2825068546
Gene: GAMT HGNC NCBI

Linked Data

ClinVar Variation Id: 853419
ClinVar RCV Id: RCV001058220
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000147.1:p.Gly175Trp
CA402994349
NM_000156.6:c.523G>T