Canonical Allele Identifier: PA2742005726
Gene: GAMT HGNC NCBI

Linked Data

ClinVar Variation Id: 2557112
ClinVar RCV Id: RCV003309105
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_620279.1:p.Thr143Ser
CA402995182
NM_138924.3:c.428C>G
CA402995197
NM_138924.3:c.427A>T