Canonical Allele Identifier: PA2825068226
Gene: GAMT HGNC NCBI

Linked Data

ClinVar Variation Id: 1444160
ClinVar RCV Id: RCV001955836

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000147.1:p.Pro4Arg
CA402998527
NM_000156.6:c.11C>G