Canonical Allele Identifier: PA2580510529
Gene: GAMT HGNC NCBI

Linked Data

ClinVar Variation Id: 2049022
ClinVar RCV Id: RCV002909488

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_620279.1:p.Ile152Met
CA402994927
NM_138924.3:c.456C>G