Canonical Allele Identifier: PA658801455
Gene: GAMT HGNC NCBI

Linked Data

ClinVar Variation Id: 544258
ClinVar RCV Id: RCV000655364
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000147.1:p.Leu177Arg
CA402994301
NM_000156.6:c.530T>G