Canonical Allele Identifier: PA2580191195
Gene: GUSB HGNC NCBI

Linked Data

ClinVar Variation Id: 1696099
ClinVar RCV Id: RCV002266243 RCV002286873
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001271219.1:p.Phe51Ile
CA367654900
NM_001284290.2:c.151T>A