Canonical Allele Identifier: PA2828805840
Gene: TRIM32 HGNC NCBI

Linked Data

ClinVar Variation Id: 260216
ClinVar RCV Id: RCV000247857 RCV000310268 RCV000364969 RCV001095303 RCV001706347
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001365978.1:p.Thr257Arg
CA5211042
NM_001379049.1:c.770C>G