Allele Registry

Canonical Allele Identifier: PA2825738963

Gene: TRIM2 HGNC NCBI

ClinVar RCV:

RCV000850295

ClinVar Variation:

689544

HGVS (amino-acid)	Matching Registered Transcripts
NP_001123539.1:p.Gly613Cys	CA358469567 NM_001130067.2:c.1837G>T