Canonical Allele Identifier: PA2828805642
Gene: TRIM32 HGNC NCBI

Linked Data

ClinVar Variation Id: 851419
ClinVar RCV Id: RCV001055811 RCV002553357 RCV003141987
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001365978.1:p.Arg33Cys
CA5210902
NM_001379049.1:c.97C>T