Canonical Allele Identifier: PA2825068486
Gene: GAMT HGNC NCBI

Linked Data

ClinVar Variation Id: 2049022
ClinVar RCV Id: RCV002909488

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000147.1:p.Ile152Met
CA402994927
NM_000156.6:c.456C>G