Canonical Allele Identifier: PA2825499550
Gene: TRIM32 HGNC NCBI

Linked Data

ClinVar Variation Id: 837259
ClinVar RCV Id: RCV001038551 RCV002479247 RCV003141949
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001093149.1:p.Arg109Trp
CA5210944
NM_001099679.2:c.325C>T