Canonical Allele Identifier: PA093729
Gene: RAB33B HGNC NCBI

Linked Data

ClinVar Variation Id: 50230
ClinVar RCV Id: RCV000043483
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_112586.1:p.Lys46Gln
CA143715
NM_031296.3:c.136A>C