Canonical Allele Identifier: PA658661676
Gene: TRIM2 HGNC NCBI

Linked Data

ClinVar Variation Id: 474608
ClinVar RCV Id: RCV000546134 RCV001584333 RCV004024290
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001123539.1:p.Ile706Val
CA3108932
NM_001130067.2:c.2116A>G