Canonical Allele Identifier: PA2825499431
Gene: TRIM32 HGNC NCBI

Linked Data

ClinVar Variation Id: 1447219
ClinVar RCV Id: RCV002011842
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001093149.1:p.Glu29Gly
CA5210898
NM_001099679.2:c.86A>G