Canonical Allele Identifier: PA916071295
Gene: GAMT HGNC NCBI

Linked Data

ClinVar Variation Id: 426381
ClinVar RCV Id: RCV000489257 RCV001856897
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_620279.1:p.Leu99Phe
CA402996261
NM_138924.3:c.295C>T