Canonical Allele Identifier: PA2826822391
Gene: GUSB HGNC NCBI

Linked Data

ClinVar Variation Id: 1051643
ClinVar RCV Id: RCV001359710
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001280033.1:p.Ile439Met
CA4276149
NM_001293104.2:c.1317T>G