Canonical Allele Identifier: PA2825068277
Gene: GAMT HGNC NCBI

Linked Data

ClinVar Variation Id: 1056003
ClinVar RCV Id: RCV001364766
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000147.1:p.Ala29Thr
CA402998231
NM_000156.6:c.85G>A