Canonical Allele Identifier: PA2580510562
Gene: GAMT HGNC NCBI

Linked Data

ClinVar Variation Id: 2055898
ClinVar RCV Id: RCV002938277

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_620279.1:p.Thr172Ile
CA9043620
NM_138924.3:c.515C>T