Canonical Allele Identifier: PA2826687845
Gene: GUSB HGNC NCBI

Linked Data

ClinVar Variation Id: 2432339
ClinVar RCV Id: RCV003135499
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001271219.1:p.Lys482Thr
CA367637231
NM_001284290.2:c.1445A>C