Canonical Allele Identifier: PA2828805082
Gene: TRIM32 HGNC NCBI

Linked Data

ClinVar Variation Id: 1312887
ClinVar RCV Id: RCV001774341
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001365977.1:p.Leu14Val
CA374647430
NM_001379048.1:c.40C>G