Canonical Allele Identifier: PA314819
Gene: GAMT HGNC NCBI

Linked Data

ClinVar Variation Id: 205587
ClinVar RCV Id: RCV000187572
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000147.1:p.Glu176Ala
CA314818
NM_000156.6:c.527A>C