Canonical Allele Identifier: PA645482281
Gene: GAMT HGNC NCBI

Linked Data

ClinVar Variation Id: 430374

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000147.1:p.Tyr137Ser
CA402995333
NM_000156.6:c.410A>C