Canonical Allele Identifier: PA2828805630
Gene: TRIM32 HGNC NCBI

Linked Data

ClinVar Variation Id: 1312887
ClinVar RCV Id: RCV001774341

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001365978.1:p.Leu14Val
CA374647430
NM_001379049.1:c.40C>G