Canonical Allele Identifier: PA2825068331
Gene: GAMT HGNC NCBI

Linked Data

ClinVar Variation Id: 1415193
ClinVar RCV Id: RCV001932962
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000147.1:p.Lys60Thr
CA402997977
NM_000156.6:c.179A>C