Allele Registry

Canonical Allele Identifier: PA2827584389

Gene: TRIM2 HGNC NCBI

ClinVar RCV:

RCV000235081

ClinVar Variation:

243075

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