Canonical Allele Identifier: PA2828806275
Gene: TRIM32 HGNC NCBI

Linked Data

ClinVar Variation Id: 1426455
ClinVar RCV Id: RCV001949738
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001365979.1:p.Glu125Gly
CA5210957
NM_001379050.1:c.374A>G