Canonical Allele Identifier: PA2825068308
Gene: GAMT HGNC NCBI

Linked Data

ClinVar Variation Id: 1304798
ClinVar RCV Id: RCV001765034

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000147.1:p.Pro48Ser
CA402998076
NM_000156.6:c.142C>T