Canonical Allele Identifier: PA314833
Gene: GAMT HGNC NCBI

Linked Data

ClinVar Variation Id: 205594
ClinVar RCV Id: RCV000187579 RCV002305457
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000147.1:p.Pro226Leu
CA314832
NM_000156.6:c.677C>T