Canonical Allele Identifier: PA916071248
Gene: GAMT HGNC NCBI

Linked Data

ClinVar Variation Id: 205601
ClinVar RCV Id: RCV000187586 RCV001833119 RCV002517863
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_620279.1:p.Met42Val
CA314846
NM_138924.3:c.124A>G