Canonical Allele Identifier: PA093739
Gene: GAMT HGNC NCBI

Linked Data

ClinVar Variation Id: 205580
ClinVar RCV Id: RCV000187565 RCV002305455 RCV002517861
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000147.1:p.Val110Phe
CA314806
NM_000156.6:c.328G>T