Canonical Allele Identifier: PA093722
Gene: GAMT HGNC NCBI

Linked Data

ClinVar Variation Id: 8303

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000147.1:p.Trp20Ser
CA340769
NM_000156.6:c.59G>C