Canonical Allele Identifier: PA645381064
Gene: TRIM32 HGNC NCBI

Linked Data

ClinVar Variation Id: 283473
ClinVar RCV Id: RCV000281057 RCV000336149 RCV000725279 RCV001516086 RCV003939975
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_036342.2:p.Arg124Trp
CA5210955
NM_012210.3:c.370C>T