Canonical Allele Identifier: PA2828805717
Gene: TRIM32 HGNC NCBI

Linked Data

ClinVar Variation Id: 411140

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001365978.1:p.Arg113Trp
CA5210948
NM_001379049.1:c.337C>T