Canonical Allele Identifier: PA916071251
Gene: GAMT HGNC NCBI

Linked Data

ClinVar Variation Id: 205602
ClinVar RCV Id: RCV000187587
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_620279.1:p.Glu43Gly
CA314848
NM_138924.3:c.128A>G