Canonical Allele Identifier: PA2826244911
Gene: TRIM22 HGNC NCBI

Linked Data

ClinVar Variation Id: 1328239
ClinVar RCV Id: RCV001795671
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001186502.1:p.Glu83Lys
CA5845734
NM_001199573.2:c.247G>A