Canonical Allele Identifier: PA916071262
Gene: GAMT HGNC NCBI

Linked Data

ClinVar Variation Id: 566179

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_620279.1:p.Met50Ile
CA402998057
NM_138924.3:c.150G>T
CA402998058
NM_138924.3:c.150G>A
CA402998059
NM_138924.3:c.150G>C