Canonical Allele Identifier: PA2825068513
Gene: GAMT HGNC NCBI

Linked Data

ClinVar Variation Id: 1312507
ClinVar RCV Id: RCV001761401
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000147.1:p.Gly164Val
CA402994587
NM_000156.6:c.491G>T