Canonical Allele Identifier: PA2825499577
Gene: TRIM32 HGNC NCBI

Linked Data

ClinVar Variation Id: 1426455
ClinVar RCV Id: RCV001949738

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001093149.1:p.Glu125Gly
CA5210957
NM_001099679.2:c.374A>G