Canonical Allele Identifier: PA645381075
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_036342.2:p.Pro137Ser
CA5210968
NM_012210.3:c.409C>T