Canonical Allele Identifier: PA2826687797
Gene: GUSB HGNC NCBI

Linked Data

ClinVar Variation Id: 193563
ClinVar RCV Id: RCV000173654 RCV003987421
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001271219.1:p.Gly366Arg
CA346856
NM_001284290.2:c.1096G>A
CA367640265
NM_001284290.2:c.1096G>C