Canonical Allele Identifier: PA2826687829
Gene: GUSB HGNC NCBI

Linked Data

ClinVar Variation Id: 1493261
ClinVar RCV Id: RCV001984237 RCV003264376
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001271219.1:p.Thr453Met
CA4276159
NM_001284290.2:c.1358C>T