Canonical Allele Identifier: PA2499297180
Gene: GAMT HGNC NCBI

Linked Data

ClinVar Variation Id: 1056003
ClinVar RCV Id: RCV001364766

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_620279.1:p.Ala29Thr
CA402998231
NM_138924.3:c.85G>A