Canonical Allele Identifier: PA2828805083
Gene: TRIM32 HGNC NCBI

Linked Data

ClinVar Variation Id: 597474

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001365977.1:p.Arg15Gln
CA374647436
NM_001379048.1:c.44G>A