Canonical Allele Identifier: PA2828805629
Gene: TRIM32 HGNC NCBI

Linked Data

ClinVar Variation Id: 934355
ClinVar RCV Id: RCV001202724
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001365978.1:p.Leu14Phe
CA5210892
NM_001379049.1:c.40C>T