Canonical Allele Identifier: PA2825068503
Gene: GAMT HGNC NCBI

Linked Data

ClinVar Variation Id: 2089224
ClinVar RCV Id: RCV003012042

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000147.1:p.Leu160Arg
CA402994675
NM_000156.6:c.479T>G