Canonical Allele Identifier: PA2828805701
Gene: TRIM32 HGNC NCBI

Linked Data

ClinVar Variation Id: 289342
ClinVar RCV Id: RCV000389877 RCV000543108 RCV001168347 RCV001168348 RCV002494885
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001365978.1:p.Leu98Ile
CA5210938
NM_001379049.1:c.292C>A