Canonical Allele Identifier: PA658801462
Gene: GAMT HGNC NCBI

Linked Data

ClinVar Variation Id: 544252
ClinVar RCV Id: RCV000655357 RCV002305524
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000147.1:p.Thr234Ile
CA402990219
NM_000156.6:c.701C>T