Allele Registry

Canonical Allele Identifier: PA2825499627

Gene: TRIM32 HGNC NCBI

ClinVar RCV:

RCV000408167

RCV001038537

RCV002494846

RCV003114447

RCV003401251

ClinVar Variation:

285227

HGVS (amino-acid)	Matching Registered Transcripts
NP_001093149.1:p.Leu156Pro	CA5210987 NM_001099679.2:c.467T>C