Canonical Allele Identifier: PA2828805169
Gene: TRIM32 HGNC NCBI

Linked Data

ClinVar Variation Id: 411140
ClinVar RCV Id: RCV000473842 RCV003139663
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001365977.1:p.Arg113Trp
CA5210948
NM_001379048.1:c.337C>T