Canonical Allele Identifier: PA2828805230
Gene: TRIM32 HGNC NCBI

Linked Data

ClinVar Variation Id: 288658
ClinVar RCV Id: RCV000473777 RCV000402475 RCV002518050 RCV002504011 RCV003401264
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001365977.1:p.Ser174Phe
CA5210998
NM_001379048.1:c.521C>T