Canonical Allele Identifier: PA645482156
Gene: GAMT HGNC NCBI

Linked Data

ClinVar Variation Id: 328350

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000147.1:p.Gly61Glu
CA9043773
NM_000156.6:c.182G>A