Canonical Allele Identifier: PA314837
Gene: GAMT HGNC NCBI

Linked Data

ClinVar Variation Id: 205596
ClinVar RCV Id: RCV000464619 RCV000711736 RCV001123244 RCV002317100
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000147.1:p.Gly236Ala
CA314836
NM_000156.6:c.707G>C