Canonical Allele Identifier: PA314839
Gene: GAMT HGNC NCBI

Linked Data

ClinVar Variation Id: 205597
ClinVar RCV Id: RCV000187582 RCV003258689 RCV001828001 RCV002517862
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000147.1:p.Ala6Val
CA314838
NM_000156.6:c.17C>T