Canonical Allele Identifier: PA2825068269
Gene: GAMT HGNC NCBI

Linked Data

ClinVar Variation Id: 2297689
ClinVar RCV Id: RCV002882425

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000147.1:p.Gly21Glu
CA402998310
NM_000156.6:c.62G>A