Canonical Allele Identifier: PA2573194858
Gene: GUSB HGNC NCBI

Linked Data

ClinVar Variation Id: 1492506
ClinVar RCV Id: RCV001981007
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001271219.1:p.Arg3Trp
CA4276764
NM_001284290.2:c.7C>T