Canonical Allele Identifier: PA2828805706
Gene: TRIM32 HGNC NCBI

Linked Data

ClinVar Variation Id: 914267
ClinVar RCV Id: RCV001168351 RCV001168352 RCV001316377
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001365978.1:p.Arg106His
CA198769340
NM_001379049.1:c.317G>A