Canonical Allele Identifier: PA645482295
Gene: GAMT HGNC NCBI

Linked Data

ClinVar Variation Id: 429874
ClinVar RCV Id: RCV000493155
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000147.1:p.Tyr168Ser
CA402994540
NM_000156.6:c.503A>C