Canonical Allele Identifier: PA2827584389
Gene: TRIM2 HGNC NCBI

Linked Data

ClinVar Variation Id: 243075
ClinVar RCV Id: RCV000235081

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001337983.1:p.Asp662Ala
CA10584080
NM_001351054.2:c.1985A>C