Allele Registry

Canonical Allele Identifier: PA2827585339

Gene: TRIM2 HGNC NCBI

ClinVar RCV:

RCV000850295

ClinVar Variation:

689544

HGVS (amino-acid)	Matching Registered Transcripts
NP_001337986.1:p.Gly488Cys	CA358469567 NM_001351057.2:c.1462G>T