Canonical Allele Identifier: PA2828805685
Gene: TRIM32 HGNC NCBI

Linked Data

ClinVar Variation Id: 167745
ClinVar RCV Id: RCV000154018 RCV000205901 RCV003390845 RCV002483329
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001365978.1:p.Ile86Thr
CA235012
NM_001379049.1:c.257T>C