Canonical Allele Identifier: PA2825499627
Gene: TRIM32 HGNC NCBI

Linked Data

ClinVar Variation Id: 285227
ClinVar RCV Id: RCV000408167 RCV001038537 RCV002494846 RCV003401251 RCV003114447
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001093149.1:p.Leu156Pro
CA5210987
NM_001099679.2:c.467T>C