Canonical Allele Identifier: PA2825068540
Gene: GAMT HGNC NCBI

Linked Data

ClinVar Variation Id: 1420866

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000147.1:p.Trp174Arg
CA304065950
NM_000156.6:c.520T>C
CA402994393
NM_000156.6:c.520T>A