Canonical Allele Identifier: PA2573300015
Gene: GAMT HGNC NCBI

Linked Data

ClinVar Variation Id: 1678192
ClinVar RCV Id: RCV002224783

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_620279.1:p.Pro8Leu
CA402998455
NM_138924.3:c.23C>T