Canonical Allele Identifier: PA916014189
Gene: GUSB HGNC NCBI

Linked Data

ClinVar Variation Id: 558975
ClinVar RCV Id: RCV000675838 RCV001309357
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001271219.1:p.Arg57Leu
CA4276735
NM_001284290.2:c.170G>T