Canonical Allele Identifier: PA658801448
Gene: GAMT HGNC NCBI

Linked Data

ClinVar Variation Id: 544260

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000147.1:p.Asn154Lys
CA402994784
NM_000156.6:c.462C>G
CA402994785
NM_000156.6:c.462C>A