Canonical Allele Identifier: PA2825068227
Gene: GAMT HGNC NCBI

Linked Data

ClinVar Variation Id: 1416096
ClinVar RCV Id: RCV001935523

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000147.1:p.Ala6Thr
CA402998496
NM_000156.6:c.16G>A