Canonical Allele Identifier: PA314849
Gene: GAMT HGNC NCBI

Linked Data

ClinVar Variation Id: 205602
ClinVar RCV Id: RCV000187587

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000147.1:p.Glu43Gly
CA314848
NM_000156.6:c.128A>G