Allele Registry

Canonical Allele Identifier: PA2827585074

Gene: TRIM2 HGNC NCBI

ClinVar RCV:

RCV000850295

ClinVar Variation:

689544

HGVS (amino-acid)	Matching Registered Transcripts
NP_001337985.1:p.Gly613Cys	CA358469567 NM_001351056.2:c.1837G>T