Canonical Allele Identifier: PA2828805631
Gene: TRIM32 HGNC NCBI

Linked Data

ClinVar Variation Id: 653096
ClinVar RCV Id: RCV000808795 RCV003141816
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001365978.1:p.Arg15Trp
CA374647435
NM_001379049.1:c.43C>T