Canonical Allele Identifier: PA2580510551
Gene: GAMT HGNC NCBI

Linked Data

ClinVar Variation Id: 2089224
ClinVar RCV Id: RCV003012042
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_620279.1:p.Leu160Arg
CA402994675
NM_138924.3:c.479T>G