Canonical Allele Identifier: PA916071296
Gene: GAMT HGNC NCBI

Linked Data

ClinVar Variation Id: 205579

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_620279.1:p.Arg100Trp
CA314802
NM_138924.3:c.298C>T