Canonical Allele Identifier: PA2825068484
Gene: GAMT HGNC NCBI

Linked Data

ClinVar Variation Id: 2066559
ClinVar RCV Id: RCV002949155
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000147.1:p.Asn150Ser
CA9043659
NM_000156.6:c.449A>G