Canonical Allele Identifier: PA2828806263
Gene: TRIM32 HGNC NCBI

Linked Data

ClinVar Variation Id: 411140

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001365979.1:p.Arg113Trp
CA5210948
NM_001379050.1:c.337C>T