Canonical Allele Identifier: PA2828805627
Gene: TRIM32 HGNC NCBI

Linked Data

ClinVar Variation Id: 864083

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001365978.1:p.Leu11Pro
CA5210890
NM_001379049.1:c.32T>C