Canonical Allele Identifier: PA1139747019
Gene: GAMT HGNC NCBI

Linked Data

ClinVar Variation Id: 856428

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_620279.1:p.Cys16Gly
CA402998372
NM_138924.3:c.46T>G