Canonical Allele Identifier: PA2825068232
Gene: GAMT HGNC NCBI

Linked Data

ClinVar Variation Id: 1678192
ClinVar RCV Id: RCV002224783

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000147.1:p.Pro8Leu
CA402998455
NM_000156.6:c.23C>T