Canonical Allele Identifier: PA2828806253
Gene: TRIM32 HGNC NCBI

Linked Data

ClinVar Variation Id: 914267
ClinVar RCV Id: RCV001168351 RCV001168352 RCV001316377
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001365979.1:p.Arg106His
CA198769340
NM_001379050.1:c.317G>A