Canonical Allele Identifier: PA2828805079
Gene: TRIM32 HGNC NCBI

Linked Data

ClinVar Variation Id: 864083
ClinVar RCV Id: RCV001071186 RCV002482140 RCV003413896 RCV004030779
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001365977.1:p.Leu11Pro
CA5210890
NM_001379048.1:c.32T>C