Canonical Allele Identifier: PA2573300008
Gene: GAMT HGNC NCBI

Linked Data

ClinVar Variation Id: 1416096
ClinVar RCV Id: RCV001935523

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_620279.1:p.Ala6Thr
CA402998496
NM_138924.3:c.16G>A