Canonical Allele Identifier: PA093578
Gene: GAMT HGNC NCBI

Linked Data

ClinVar Variation Id: 2446454
ClinVar RCV Id: RCV003159288

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000147.1:p.Ala54Pro
CA402998035
NM_000156.6:c.160G>C