Canonical Allele Identifier: PA645508767
Gene: RAB28 HGNC NCBI

Linked Data

ClinVar Variation Id: 225879
ClinVar RCV Id: RCV000211107 RCV001300998
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004240.2:p.Cys217Trp
CA2859979
NM_004249.4:c.651T>G