Canonical Allele Identifier: PA2828805942
Gene: TRIM32 HGNC NCBI

Linked Data

ClinVar Variation Id: 501836
ClinVar RCV Id: RCV000593588
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001365978.1:p.Gly365Ser
CA374650939
NM_001379049.1:c.1093G>A