Canonical Allele Identifier: PA103479
Gene: TRIM2 HGNC NCBI

Linked Data

ClinVar Variation Id: 83303
ClinVar RCV Id: RCV000074302
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001123539.1:p.Glu227Val
CA211304
NM_001130067.2:c.680A>T