Canonical Allele Identifier: PA2825499993
Gene: TRIM32 HGNC NCBI

Linked Data

ClinVar Variation Id: 100583
ClinVar RCV Id: RCV000086966 RCV000244938 RCV000626297 RCV001084393 RCV001166672
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001093149.1:p.Arg408Cys
CA228919
NM_001099679.2:c.1222C>T