Canonical Allele Identifier: PA2825068481
Gene: GAMT HGNC NCBI

Linked Data

ClinVar Variation Id: 978187
ClinVar RCV Id: RCV001256148

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000147.1:p.Thr146Arg
CA9043661
NM_000156.6:c.437C>G