Canonical Allele Identifier: PA2828805985
Gene: TRIM32 HGNC NCBI

Linked Data

ClinVar Variation Id: 100583
ClinVar RCV Id: RCV000086966 RCV000244938 RCV000626297 RCV001084393 RCV001166672
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001365978.1:p.Arg408Cys
CA228919
NM_001379049.1:c.1222C>T