Canonical Allele Identifier: PA2825068477
Gene: GAMT HGNC NCBI

Linked Data

ClinVar Variation Id: 2557112
ClinVar RCV Id: RCV003309105

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000147.1:p.Thr143Ser
CA402995182
NM_000156.6:c.428C>G
CA402995197
NM_000156.6:c.427A>T