Canonical Allele Identifier: PA916071237
Gene: GAMT HGNC NCBI

Linked Data

ClinVar Variation Id: 588631
ClinVar RCV Id: RCV001051211 RCV002307606 RCV002313571 RCV003334006
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_620279.1:p.Trp20Leu
CA402998326
NM_138924.3:c.59G>T