Canonical Allele Identifier: PA2825499564
Gene: TRIM32 HGNC NCBI

Linked Data

ClinVar Variation Id: 1339315
ClinVar RCV Id: RCV001823838 RCV001869825 RCV003923332
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001093149.1:p.Ser114Asn
CA5210951
NM_001099679.2:c.341G>A