Canonical Allele Identifier: PA2828806249
Gene: TRIM32 HGNC NCBI

Linked Data

ClinVar Variation Id: 289342

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001365979.1:p.Leu98Ile
CA5210938
NM_001379050.1:c.292C>A