Canonical Allele Identifier: PA093642
Gene: GAMT HGNC NCBI

Linked Data

ClinVar Variation Id: 205581
ClinVar RCV Id: RCV000187566 RCV001731508 RCV002305456 RCV001300727 RCV002345673
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000147.1:p.Gly164Asp
CA314807
NM_000156.6:c.491G>A