Canonical Allele Identifier: PA1139717725
Gene: TRIM32 HGNC NCBI

Linked Data

ClinVar Variation Id: 864083

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_036342.2:p.Leu11Pro
CA5210890
NM_012210.3:c.32T>C