Canonical Allele Identifier: PA645381022
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_036342.2:p.Leu98Ile
CA5210938
NM_012210.3:c.292C>A