Allele Registry

Canonical Allele Identifier: PA2827584729

Gene: TRIM2 HGNC NCBI

ClinVar RCV:

RCV000850295

ClinVar Variation:

689544

HGVS (amino-acid)	Matching Registered Transcripts
NP_001337984.1:p.Gly630Cys	CA358469567 NM_001351055.2:c.1888G>T