Canonical Allele Identifier: PA2825068249
Gene: GAMT HGNC NCBI

Linked Data

ClinVar Variation Id: 2097428
ClinVar RCV Id: RCV003016696

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000147.1:p.Gly13Cys
CA402998401
NM_000156.6:c.37G>T