Canonical Allele Identifier: PA099508
Gene: TRIM32 HGNC NCBI

Linked Data

ClinVar Variation Id: 7353
ClinVar RCV Id: RCV000007778 RCV000362326 RCV000638363 RCV001334685
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001093149.1:p.Arg394His
CA118731
NM_001099679.2:c.1181G>A