Canonical Allele Identifier: PA645381032
Gene: TRIM32 HGNC NCBI

Linked Data

ClinVar Variation Id: 411140

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_036342.2:p.Arg113Trp
CA5210948
NM_012210.3:c.337C>T