Canonical Allele Identifier: PA913198330
Gene: TRIM32 HGNC NCBI

Linked Data

ClinVar Variation Id: 597474
ClinVar RCV Id: RCV000733607 RCV001060210
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_036342.2:p.Arg15Gln
CA374647436
NM_012210.3:c.44G>A