Canonical Allele Identifier: PA645427012
Gene: RAB33B HGNC NCBI

Linked Data

ClinVar Variation Id: 425561
ClinVar RCV Id: RCV000488435
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_112586.1:p.Phe122Ser
CA358272776
NM_031296.3:c.365T>C