Canonical Allele Identifier: PA2825068518
Gene: GAMT HGNC NCBI

Linked Data

ClinVar Variation Id: 2743645
ClinVar RCV Id: RCV003587559
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000147.1:p.Tyr168_Thr172del
CA2697555584
NM_000156.6:c.503_517del