Allele Registry

Canonical Allele Identifier: PA2827584189

Gene: TRIM2 HGNC NCBI

ClinVar RCV:

RCV000074302

ClinVar Variation:

83303

HGVS (amino-acid)	Matching Registered Transcripts
NP_001337983.1:p.Glu245Val	CA211304 NM_001351054.2:c.734A>T