Canonical Allele Identifier: PA2826687623
Gene: GUSB HGNC NCBI

Linked Data

ClinVar Variation Id: 3064887
ClinVar RCV Id: RCV003989964
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001271219.1:p.Trp63Cys
CA367654647
NM_001284290.2:c.189G>T
CA367654652
NM_001284290.2:c.189G>C