Allele Registry

Canonical Allele Identifier: PA915979195

Gene: TRIM2 HGNC NCBI

ClinVar RCV:

RCV000074302

ClinVar Variation:

83303

HGVS (amino-acid)	Matching Registered Transcripts
NP_056086.2:p.Glu254Val	CA211304 NM_015271.5:c.761A>T