Canonical Allele Identifier: PA916071238
Gene: GAMT HGNC NCBI

Linked Data

ClinVar Variation Id: 8303

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_620279.1:p.Trp20Ser
CA340769
NM_138924.3:c.59G>C