Canonical Allele Identifier: PA891845840
Gene: GAMT HGNC NCBI

Linked Data

ClinVar Variation Id: 569288
ClinVar RCV Id: RCV000689882
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000147.1:p.Pro40Leu
CA402998123
NM_000156.6:c.119C>T