Allele Registry

Canonical Allele Identifier: PA103479

Gene: TRIM2 HGNC NCBI

ClinVar RCV:

RCV000074302

ClinVar Variation:

83303

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