Canonical Allele Identifier: PA102484
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_060547.2:p.Leu351Pro
CA114462
NM_018077.3:c.1052T>C