Canonical Allele Identifier: PA2826687836
Gene: GUSB HGNC NCBI
ClinVar RCV:
RCV000000945
ClinVar Variation:
897
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001271219.1:p.Arg465Trp
CA339841
NM_001284290.2:c.1393C>T