Canonical Allele Identifier: PA2828806182
Gene: TRIM32 HGNC NCBI

Linked Data

ClinVar Variation Id: 2133643
ClinVar RCV Id: RCV003056345

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001365979.1:p.Glu19Ala
CA374647459
NM_001379050.1:c.56A>C