Canonical Allele Identifier: PA2825068532
Gene: GAMT HGNC NCBI

Linked Data

ClinVar Variation Id: 2055898
ClinVar RCV Id: RCV002938277
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000147.1:p.Thr172Ile
CA9043620
NM_000156.6:c.515C>T