Canonical Allele Identifier: PA2825499597
Gene: TRIM32 HGNC NCBI

Linked Data

ClinVar Variation Id: 364717
ClinVar RCV Id: RCV000304291 RCV000398363 RCV001095348 RCV001558645 RCV003950293
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001093149.1:p.Pro137Ser
CA5210968
NM_001099679.2:c.409C>T