Canonical Allele Identifier: PA2826687853
Gene: GUSB HGNC NCBI

Linked Data

ClinVar Variation Id: 911767
ClinVar RCV Id: RCV001164418
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001271219.1:p.Ser492Pro
CA367637101
NM_001284290.2:c.1474T>C