Canonical Allele Identifier: PA2825068289
Gene: GAMT HGNC NCBI

Linked Data

ClinVar Variation Id: 2143904
ClinVar RCV Id: RCV003053201

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000147.1:p.Gly38Ser
CA304067308
NM_000156.6:c.112G>A