Canonical Allele Identifier: PA2825068292
Gene: GAMT HGNC NCBI

Linked Data

ClinVar Variation Id: 1051517
ClinVar RCV Id: RCV001359569

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000147.1:p.Lys39Gln
CA402998135
NM_000156.6:c.115A>C