Canonical Allele Identifier: PA2826024929
Gene: RBM28 HGNC NCBI

Linked Data

ClinVar Variation Id: 732
ClinVar RCV Id: RCV000000768
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001159607.1:p.Leu210Pro
CA114462
NM_001166135.1:c.629T>C